SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45332801A>C , CM000663.2:g.45332801A>C | GRCh38 |
| NC_000001.10:g.45798473A>C , CM000663.1:g.45798473A>C | GRCh37 |
| NC_000001.9:g.45571060A>C | NCBI36 |
| NG_008189.1:g.12670T>G , LRG_220:g.12670T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412971.6:c.70T>G | ENSP00000410263.2:p.Tyr24Asp | |
| ENST00000435155.2:c.487T>G | ENSP00000403655.2:p.Tyr163Asp | |
| ENST00000467459.6:c.454T>G | ENSP00000435889.2:p.Tyr152Asp | |
| ENST00000483127.2:c.472T>G | ENSP00000436469.2:p.Tyr158Asp | |
| ENST00000485271.6:c.454T>G | ENSP00000431264.2:p.Tyr152Asp | |
| ENST00000529892.6:c.496T>G | ENSP00000432528.2:p.Tyr166Asp | |
| ENST00000533178.6:c.116-114T>G | ENSP00000436430.2:n.116-114T>G | |
| ENST00000672314.2:c.454T>G | ENSP00000500828.2:p.Tyr152Asp | |
| ENST00000674679.2:c.*366T>G | ENSP00000501623.2:n.*366T>G | |
| ENST00000710952.2:c.538T>G MANE Plus Clinical | ENSP00000518552.2:p.Tyr180Asp | |
| ENST00000672818.3:c.529T>G | ENSP00000500891.1:p.Tyr177Asp | |
| ENST00000450313.6:c.464T>G | ENSP00000408176.2:p.Leu155Arg | |
| ENST00000456914.7:c.454T>G MANE Select | ENSP00000407590.2:p.Tyr152Asp | |
| ENST00000461495.6:c.*193T>G | ENSP00000437166.1:n.*193T>G | |
| ENST00000671856.1:n.400T>G | ||
| ENST00000671898.1:c.1042T>G | ENSP00000499896.1:p.Tyr348Asp | |
| ENST00000672011.1:c.422T>G | ENSP00000500418.1:p.Leu141Arg | |
| ENST00000672314.1:c.454T>G | ENSP00000500828.1:p.Tyr152Asp | |
| ENST00000672593.1:c.*267T>G | ENSP00000500455.1:n.*267T>G | |
| ENST00000672764.1:c.413T>G | ENSP00000500886.1:p.Leu138Arg | |
| ENST00000672818.2:c.529T>G | ENSP00000500891.1:p.Tyr177Asp | |
| ENST00000673134.1:c.*151T>G | ENSP00000500526.1:n.*151T>G | |
| ENST00000674679.1:c.482T>G | ENSP00000501623.1:n.482T>G | |
| ENST00000354383.10:c.457T>G | ENSP00000346354.6:p.Tyr153Asp | |
| ENST00000355498.6:c.454T>G | ENSP00000347685.2:p.Tyr152Asp | |
| ENST00000372098.7:c.529T>G | ENSP00000361170.3:p.Tyr177Asp | |
| ENST00000372104.5:c.454T>G | ENSP00000361176.1:p.Tyr152Asp | |
| ENST00000372110.7:c.499T>G | ENSP00000361182.3:p.Tyr167Asp | |
| ENST00000372115.7:c.496T>G | ENSP00000361187.3:p.Tyr166Asp | |
| ENST00000412971.5:c.70T>G | ENSP00000410263.1:p.Tyr24Asp | |
| ENST00000435155.1:c.487T>G | ENSP00000403655.1:p.Tyr163Asp | |
| ENST00000448481.5:c.487T>G | ENSP00000409718.1:p.Tyr163Asp | |
| ENST00000450313.5:c.538T>G | ENSP00000408176.1:p.Tyr180Asp | |
| ENST00000456914.6:c.454T>G | ENSP00000407590.2:p.Tyr152Asp | |
| ENST00000461495.5:c.*193T>G | ENSP00000437166.1:n.*193T>G | |
| ENST00000462388.5:n.145T>G | ||
| ENST00000467940.5:c.*377T>G | ENSP00000436478.1:n.*377T>G | |
| ENST00000470256.5:c.341T>G | ENSP00000434985.1:p.Leu114Arg | |
| ENST00000475516.5:c.*267T>G | ENSP00000433843.1:n.*267T>G | |
| ENST00000476789.5:n.894T>G | ||
| ENST00000478796.5:n.441T>G | ||
| ENST00000479746.6:n.737T>G | ||
| ENST00000481139.5:n.927T>G | ||
| ENST00000481571.5:c.*267T>G | ENSP00000436597.1:n.*267T>G | |
| ENST00000483642.5:n.969T>G | ||
| ENST00000485484.5:n.755T>G | ||
| ENST00000488731.6:c.149T>G | ENSP00000432330.1:p.Leu50Arg | |
| ENST00000492494.5:n.851T>G | ||
| ENST00000525160.5:c.*105T>G | ENSP00000431568.1:n.*105T>G | |
| ENST00000528013.6:c.496T>G | ENSP00000433130.2:p.Tyr166Asp | |
| ENST00000529984.5:c.149T>G | ENSP00000437093.1:p.Leu50Arg | |
| ENST00000531105.5:c.115+1590T>G | ENSP00000431292.1:n.115+1590T>G | |
| ENST00000533178.5:c.122-114T>G | ENSP00000436430.1:n.122-114T>G | |
| NM_001048171.1:c.496T>G | NP_001041636.1:p.Tyr166Asp | |
| NM_001048172.1:c.457T>G | NP_001041637.1:p.Tyr153Asp | |
| NM_001048173.1:c.454T>G | NP_001041638.1:p.Tyr152Asp | |
| NM_001048174.1:c.454T>G | NP_001041639.1:p.Tyr152Asp | |
| NM_001128425.1:c.538T>G , LRG_220t1:c.538T>G | NP_001121897.1:p.Tyr180Asp | |
| NM_001293190.1:c.499T>G | NP_001280119.1:p.Tyr167Asp | |
| NM_001293191.1:c.487T>G | NP_001280120.1:p.Tyr163Asp | |
| NM_001293192.1:c.178T>G | NP_001280121.1:p.Tyr60Asp | |
| NM_001293195.1:c.454T>G | NP_001280124.1:p.Tyr152Asp | |
| NM_001293196.1:c.178T>G | NP_001280125.1:p.Tyr60Asp | |
| NM_012222.2:c.529T>G | NP_036354.1:p.Tyr177Asp | |
| XM_011541497.1:c.514T>G | XP_011539799.1:p.Tyr172Asp | |
| XM_011541498.1:c.496T>G | XP_011539800.1:p.Tyr166Asp | |
| XM_011541499.1:c.496T>G | XP_011539801.1:p.Tyr166Asp | |
| XM_011541500.1:c.496T>G | XP_011539802.1:p.Tyr166Asp | |
| XM_011541501.1:c.496T>G | XP_011539803.1:p.Tyr166Asp | |
| XM_011541502.1:c.496T>G | XP_011539804.1:p.Tyr166Asp | |
| XM_011541503.1:c.496T>G | XP_011539805.1:p.Tyr166Asp | |
| XM_011541504.1:c.487T>G | XP_011539806.1:p.Tyr163Asp | |
| XM_011541505.1:c.76T>G | XP_011539807.1:p.Tyr26Asp | |
| XM_011541506.1:c.76T>G | XP_011539808.1:p.Tyr26Asp | |
| XM_011541507.1:c.67T>G | XP_011539809.1:p.Tyr23Asp | |
| XM_011541508.1:c.82T>G | XP_011539810.1:p.Tyr28Asp | |
| XR_946658.1:n.585T>G | ||
| NM_001350650.1:c.109T>G | NP_001337579.1:p.Tyr37Asp | |
| NM_001350651.1:c.109T>G | NP_001337580.1:p.Tyr37Asp | |
| NR_146882.1:n.712T>G | ||
| NR_146883.1:n.526T>G | ||
| XM_011541497.3:c.514T>G | XP_011539799.1:p.Tyr172Asp | |
| XM_011541500.3:c.496T>G | XP_011539802.1:p.Tyr166Asp | |
| XM_011541501.2:c.496T>G | XP_011539803.1:p.Tyr166Asp | |
| XM_011541502.2:c.496T>G | XP_011539804.1:p.Tyr166Asp | |
| XM_011541503.2:c.496T>G | XP_011539805.1:p.Tyr166Asp | |
| XM_011541504.2:c.487T>G | XP_011539806.1:p.Tyr163Asp | |
| XM_011541505.2:c.76T>G | XP_011539807.1:p.Tyr26Asp | |
| XM_011541506.2:c.76T>G | XP_011539808.1:p.Tyr26Asp | |
| XM_017001331.1:c.496T>G | XP_016856820.1:p.Tyr166Asp | |
| XM_017001332.1:c.496T>G | XP_016856821.1:p.Tyr166Asp | |
| XM_017001333.1:c.496T>G | XP_016856822.1:p.Tyr166Asp | |
| XM_017001334.1:c.457T>G | XP_016856823.1:p.Tyr153Asp | |
| XM_017001335.1:c.178T>G | XP_016856824.1:p.Tyr60Asp | |
| XM_017001336.1:c.109T>G | XP_016856825.1:p.Tyr37Asp | |
| XM_017001337.1:c.109T>G | XP_016856826.1:p.Tyr37Asp | |
| XM_024447244.1:c.109T>G | XP_024303012.1:p.Tyr37Asp | |
| XM_024447245.1:c.109T>G | XP_024303013.1:p.Tyr37Asp | |
| XM_024447248.1:c.67T>G | XP_024303016.1:p.Tyr23Asp | |
| XM_024447249.1:c.-63T>G | XP_024303017.1:n.-63T>G | |
| XM_024447250.1:c.-63T>G | XP_024303018.1:n.-63T>G | |
| XM_024447251.1:c.-63T>G | XP_024303019.1:n.-63T>G | |
| XR_001737190.1:n.499T>G | ||
| XR_001737192.1:n.311T>G | ||
| XR_002956643.1:n.491T>G | ||
| XR_002956644.1:n.1026T>G | ||
| XR_946658.2:n.599T>G | ||
| NM_001048171.2:c.454T>G | NP_001041636.2:p.Tyr152Asp | |
| NM_001128425.2:c.538T>G MANE Plus Clinical | NP_001121897.1:p.Tyr180Asp | |
| NM_001048172.2:c.457T>G | NP_001041637.1:p.Tyr153Asp | |
| NM_001048173.2:c.454T>G | NP_001041638.1:p.Tyr152Asp | |
| NM_001048174.2:c.454T>G MANE Select | NP_001041639.1:p.Tyr152Asp | |
| NM_001293190.2:c.499T>G | NP_001280119.1:p.Tyr167Asp | |
| NM_001293191.2:c.487T>G | NP_001280120.1:p.Tyr163Asp | |
| NM_001293192.2:c.178T>G | NP_001280121.1:p.Tyr60Asp | |
| NM_001293195.2:c.454T>G | NP_001280124.1:p.Tyr152Asp | |
| NM_001293196.2:c.178T>G | NP_001280125.1:p.Tyr60Asp | |
| NM_001350650.2:c.109T>G | NP_001337579.1:p.Tyr37Asp | |
| NM_001350651.2:c.109T>G | NP_001337580.1:p.Tyr37Asp | |
| NM_012222.3:c.529T>G | NP_036354.1:p.Tyr177Asp | |
| NR_146882.2:n.682T>G | ||
| NR_146883.2:n.531T>G |