Linked Data
ClinVar Variation Id:
492054
dbSNP Id:
rs778899897
ExAC:
1:45798282 G / A
gnomAD v2:
1-45798282-G-A
gnomAD v4:
1-45332610-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45332610G>A , CM000663.2:g.45332610G>A | GRCh38 |
| NC_000001.10:g.45798282G>A , CM000663.1:g.45798282G>A | GRCh37 |
| NC_000001.9:g.45570869G>A | NCBI36 |
| NG_008189.1:g.12861C>T , LRG_220:g.12861C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412971.6:c.186C>T | ENSP00000410263.2:p.Tyr62= | |
| ENST00000435155.2:c.603C>T | ENSP00000403655.2:p.Tyr201= | |
| ENST00000467459.6:c.570C>T | ENSP00000435889.2:p.Tyr190= | |
| ENST00000483127.2:c.588C>T | ENSP00000436469.2:p.Tyr196= | |
| ENST00000485271.6:c.570C>T | ENSP00000431264.2:p.Tyr190= | |
| ENST00000529892.6:c.612C>T | ENSP00000432528.2:p.Tyr204= | |
| ENST00000533178.6:c.193C>T | ENSP00000436430.2:p.His65Tyr | |
| ENST00000672314.2:c.570C>T | ENSP00000500828.2:p.Tyr190= | |
| ENST00000674679.2:c.*482C>T | ENSP00000501623.2:n.*482C>T | |
| ENST00000710952.2:c.654C>T MANE Plus Clinical | ENSP00000518552.2:p.Tyr218= | |
| ENST00000672818.3:c.645C>T | ENSP00000500891.1:p.Tyr215= | |
| ENST00000450313.6:c.580C>T | ENSP00000408176.2:p.His194Tyr | |
| ENST00000456914.7:c.570C>T MANE Select | ENSP00000407590.2:p.Tyr190= | |
| ENST00000461495.6:c.*309C>T | ENSP00000437166.1:n.*309C>T | |
| ENST00000671856.1:n.516C>T | ||
| ENST00000671898.1:c.1158C>T | ENSP00000499896.1:p.Tyr386= | |
| ENST00000672011.1:c.538C>T | ENSP00000500418.1:p.His180Tyr | |
| ENST00000672314.1:c.570C>T | ENSP00000500828.1:p.Tyr190= | |
| ENST00000672593.1:c.*458C>T | ENSP00000500455.1:n.*458C>T | |
| ENST00000672764.1:c.529C>T | ENSP00000500886.1:p.His177Tyr | |
| ENST00000672818.2:c.645C>T | ENSP00000500891.1:p.Tyr215= | |
| ENST00000673134.1:c.*267C>T | ENSP00000500526.1:n.*267C>T | |
| ENST00000674679.1:c.598C>T | ENSP00000501623.1:n.598C>T | |
| ENST00000354383.10:c.573C>T | ENSP00000346354.6:p.Tyr191= | |
| ENST00000355498.6:c.570C>T | ENSP00000347685.2:p.Tyr190= | |
| ENST00000372098.7:c.645C>T | ENSP00000361170.3:p.Tyr215= | |
| ENST00000372104.5:c.570C>T | ENSP00000361176.1:p.Tyr190= | |
| ENST00000372110.7:c.615C>T | ENSP00000361182.3:p.Tyr205= | |
| ENST00000372115.7:c.612C>T | ENSP00000361187.3:p.Tyr204= | |
| ENST00000412971.5:c.186C>T | ENSP00000410263.1:p.Tyr62= | |
| ENST00000435155.1:c.603C>T | ENSP00000403655.1:p.Tyr201= | |
| ENST00000448481.5:c.603C>T | ENSP00000409718.1:p.Tyr201= | |
| ENST00000450313.5:c.654C>T | ENSP00000408176.1:p.Tyr218= | |
| ENST00000456914.6:c.570C>T | ENSP00000407590.2:p.Tyr190= | |
| ENST00000461495.5:c.*309C>T | ENSP00000437166.1:n.*309C>T | |
| ENST00000462388.5:n.261C>T | ||
| ENST00000467940.5:c.*493C>T | ENSP00000436478.1:n.*493C>T | |
| ENST00000470256.5:c.457C>T | ENSP00000434985.1:p.His153Tyr | |
| ENST00000475516.5:c.*383C>T | ENSP00000433843.1:n.*383C>T | |
| ENST00000478796.5:n.557C>T | ||
| ENST00000479746.6:n.928C>T | ||
| ENST00000481571.5:c.*383C>T | ENSP00000436597.1:n.*383C>T | |
| ENST00000488731.6:c.187+153C>T | ENSP00000432330.1:n.187+153C>T | |
| ENST00000492494.5:n.967C>T | ||
| ENST00000525160.5:c.*221C>T | ENSP00000431568.1:n.*221C>T | |
| ENST00000528013.6:c.612C>T | ENSP00000433130.2:p.Tyr204= | |
| ENST00000529984.5:c.187+153C>T | ENSP00000437093.1:n.187+153C>T | |
| ENST00000531105.5:c.115+1781C>T | ENSP00000431292.1:n.115+1781C>T | |
| ENST00000533178.5:c.199C>T | ENSP00000436430.1:p.His67Tyr | |
| NM_001048171.1:c.612C>T | NP_001041636.1:p.Tyr204= | |
| NM_001048172.1:c.573C>T | NP_001041637.1:p.Tyr191= | |
| NM_001048173.1:c.570C>T | NP_001041638.1:p.Tyr190= | |
| NM_001048174.1:c.570C>T | NP_001041639.1:p.Tyr190= | |
| NM_001128425.1:c.654C>T , LRG_220t1:c.654C>T | NP_001121897.1:p.Tyr218= | |
| NM_001293190.1:c.615C>T | NP_001280119.1:p.Tyr205= | |
| NM_001293191.1:c.603C>T | NP_001280120.1:p.Tyr201= | |
| NM_001293192.1:c.294C>T | NP_001280121.1:p.Tyr98= | |
| NM_001293195.1:c.570C>T | NP_001280124.1:p.Tyr190= | |
| NM_001293196.1:c.294C>T | NP_001280125.1:p.Tyr98= | |
| NM_012222.2:c.645C>T | NP_036354.1:p.Tyr215= | |
| XM_011541497.1:c.630C>T | XP_011539799.1:p.Tyr210= | |
| XM_011541498.1:c.612C>T | XP_011539800.1:p.Tyr204= | |
| XM_011541499.1:c.612C>T | XP_011539801.1:p.Tyr204= | |
| XM_011541500.1:c.612C>T | XP_011539802.1:p.Tyr204= | |
| XM_011541501.1:c.612C>T | XP_011539803.1:p.Tyr204= | |
| XM_011541502.1:c.612C>T | XP_011539804.1:p.Tyr204= | |
| XM_011541503.1:c.612C>T | XP_011539805.1:p.Tyr204= | |
| XM_011541504.1:c.603C>T | XP_011539806.1:p.Tyr201= | |
| XM_011541505.1:c.192C>T | XP_011539807.1:p.Tyr64= | |
| XM_011541506.1:c.192C>T | XP_011539808.1:p.Tyr64= | |
| XM_011541507.1:c.183C>T | XP_011539809.1:p.Tyr61= | |
| XM_011541508.1:c.198C>T | XP_011539810.1:p.Tyr66= | |
| XR_946658.1:n.701C>T | ||
| NM_001350650.1:c.225C>T | NP_001337579.1:p.Tyr75= | |
| NM_001350651.1:c.225C>T | NP_001337580.1:p.Tyr75= | |
| NR_146882.1:n.828C>T | ||
| NR_146883.1:n.642C>T | ||
| XM_011541497.3:c.630C>T | XP_011539799.1:p.Tyr210= | |
| XM_011541500.3:c.612C>T | XP_011539802.1:p.Tyr204= | |
| XM_011541501.2:c.612C>T | XP_011539803.1:p.Tyr204= | |
| XM_011541502.2:c.612C>T | XP_011539804.1:p.Tyr204= | |
| XM_011541503.2:c.612C>T | XP_011539805.1:p.Tyr204= | |
| XM_011541504.2:c.603C>T | XP_011539806.1:p.Tyr201= | |
| XM_011541505.2:c.192C>T | XP_011539807.1:p.Tyr64= | |
| XM_011541506.2:c.192C>T | XP_011539808.1:p.Tyr64= | |
| XM_017001331.1:c.612C>T | XP_016856820.1:p.Tyr204= | |
| XM_017001332.1:c.612C>T | XP_016856821.1:p.Tyr204= | |
| XM_017001333.1:c.612C>T | XP_016856822.1:p.Tyr204= | |
| XM_017001334.1:c.573C>T | XP_016856823.1:p.Tyr191= | |
| XM_017001335.1:c.294C>T | XP_016856824.1:p.Tyr98= | |
| XM_017001336.1:c.225C>T | XP_016856825.1:p.Tyr75= | |
| XM_017001337.1:c.225C>T | XP_016856826.1:p.Tyr75= | |
| XM_024447244.1:c.225C>T | XP_024303012.1:p.Tyr75= | |
| XM_024447245.1:c.225C>T | XP_024303013.1:p.Tyr75= | |
| XM_024447248.1:c.183C>T | XP_024303016.1:p.Tyr61= | |
| XM_024447249.1:c.54C>T | XP_024303017.1:p.Tyr18= | |
| XM_024447250.1:c.54C>T | XP_024303018.1:p.Tyr18= | |
| XM_024447251.1:c.54C>T | XP_024303019.1:p.Tyr18= | |
| XR_001737190.1:n.615C>T | ||
| XR_001737192.1:n.427C>T | ||
| XR_002956643.1:n.607C>T | ||
| XR_002956644.1:n.1142C>T | ||
| XR_946658.2:n.715C>T | ||
| NM_001048171.2:c.570C>T | NP_001041636.2:p.Tyr190= | |
| NM_001128425.2:c.654C>T MANE Plus Clinical | NP_001121897.1:p.Tyr218= | |
| NM_001048172.2:c.573C>T | NP_001041637.1:p.Tyr191= | |
| NM_001048173.2:c.570C>T | NP_001041638.1:p.Tyr190= | |
| NM_001048174.2:c.570C>T MANE Select | NP_001041639.1:p.Tyr190= | |
| NM_001293190.2:c.615C>T | NP_001280119.1:p.Tyr205= | |
| NM_001293191.2:c.603C>T | NP_001280120.1:p.Tyr201= | |
| NM_001293192.2:c.294C>T | NP_001280121.1:p.Tyr98= | |
| NM_001293195.2:c.570C>T | NP_001280124.1:p.Tyr190= | |
| NM_001293196.2:c.294C>T | NP_001280125.1:p.Tyr98= | |
| NM_001350650.2:c.225C>T | NP_001337579.1:p.Tyr75= | |
| NM_001350651.2:c.225C>T | NP_001337580.1:p.Tyr75= | |
| NM_012222.3:c.645C>T | NP_036354.1:p.Tyr215= | |
| NR_146882.2:n.798C>T | ||
| NR_146883.2:n.647C>T |