Linked Data
ClinVar Variation Id:
141994
dbSNP Id:
rs587782165
ExAC:
1:45798780 C / T
gnomAD v2:
1-45798780-C-T
gnomAD v3:
1-45333108-C-T
gnomAD v4:
1-45333108-C-T
COSMIC:
COSM1343047
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45333108C>T , CM000663.2:g.45333108C>T | GRCh38 |
| NC_000001.10:g.45798780C>T , CM000663.1:g.45798780C>T | GRCh37 |
| NC_000001.9:g.45571367C>T | NCBI36 |
| NG_008189.1:g.12363G>A , LRG_220:g.12363G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412971.6:c.37-274G>A | ENSP00000410263.2:n.37-274G>A | |
| ENST00000435155.2:c.400G>A | ENSP00000403655.2:p.Gly134Arg | |
| ENST00000467459.6:c.367G>A | ENSP00000435889.2:p.Gly123Arg | |
| ENST00000483127.2:c.385G>A | ENSP00000436469.2:p.Gly129Arg | |
| ENST00000485271.6:c.367G>A | ENSP00000431264.2:p.Gly123Arg | |
| ENST00000529892.6:c.409G>A | ENSP00000432528.2:p.Gly137Arg | |
| ENST00000533178.6:c.116-421G>A | ENSP00000436430.2:n.116-421G>A | |
| ENST00000672314.2:c.367G>A | ENSP00000500828.2:p.Gly123Arg | |
| ENST00000674679.2:c.*279G>A | ENSP00000501623.2:n.*279G>A | |
| ENST00000710952.2:c.451G>A MANE Plus Clinical | ENSP00000518552.2:p.Gly151Arg | |
| ENST00000672818.3:c.442G>A | ENSP00000500891.1:p.Gly148Arg | |
| ENST00000450313.6:c.389-149G>A | ENSP00000408176.2:n.389-149G>A | |
| ENST00000456914.7:c.367G>A MANE Select | ENSP00000407590.2:p.Gly123Arg | |
| ENST00000461495.6:c.*118-149G>A | ENSP00000437166.1:n.*118-149G>A | |
| ENST00000671856.1:n.325-149G>A | ||
| ENST00000671898.1:c.955G>A | ENSP00000499896.1:p.Gly319Arg | |
| ENST00000672011.1:c.347-149G>A | ENSP00000500418.1:n.347-149G>A | |
| ENST00000672314.1:c.367G>A | ENSP00000500828.1:p.Gly123Arg | |
| ENST00000672593.1:c.*180G>A | ENSP00000500455.1:n.*180G>A | |
| ENST00000672764.1:c.338-149G>A | ENSP00000500886.1:n.338-149G>A | |
| ENST00000672818.2:c.442G>A | ENSP00000500891.1:p.Gly148Arg | |
| ENST00000673134.1:c.*117+177G>A | ENSP00000500526.1:n.*117+177G>A | |
| ENST00000674679.1:c.395G>A | ENSP00000501623.1:n.395G>A | |
| ENST00000354383.10:c.370G>A | ENSP00000346354.6:p.Gly124Arg | |
| ENST00000355498.6:c.367G>A | ENSP00000347685.2:p.Gly123Arg | |
| ENST00000372098.7:c.442G>A | ENSP00000361170.3:p.Gly148Arg | |
| ENST00000372104.5:c.367G>A | ENSP00000361176.1:p.Gly123Arg | |
| ENST00000372110.7:c.412G>A | ENSP00000361182.3:p.Gly138Arg | |
| ENST00000372115.7:c.409G>A | ENSP00000361187.3:p.Gly137Arg | |
| ENST00000412971.5:c.37-274G>A | ENSP00000410263.1:n.37-274G>A | |
| ENST00000435155.1:c.400G>A | ENSP00000403655.1:p.Gly134Arg | |
| ENST00000448481.5:c.400G>A | ENSP00000409718.1:p.Gly134Arg | |
| ENST00000450313.5:c.451G>A | ENSP00000408176.1:p.Gly151Arg | |
| ENST00000456914.6:c.367G>A | ENSP00000407590.2:p.Gly123Arg | |
| ENST00000461495.5:c.*118-149G>A | ENSP00000437166.1:n.*118-149G>A | |
| ENST00000462387.5:n.552G>A | ||
| ENST00000467940.5:c.*290G>A | ENSP00000436478.1:n.*290G>A | |
| ENST00000470256.5:c.307+177G>A | ENSP00000434985.1:n.307+177G>A | |
| ENST00000474703.1:n.522G>A | ||
| ENST00000475516.5:c.*180G>A | ENSP00000433843.1:n.*180G>A | |
| ENST00000476789.5:n.587G>A | ||
| ENST00000478796.5:n.217G>A | ||
| ENST00000479746.6:n.430G>A | ||
| ENST00000481139.5:n.620G>A | ||
| ENST00000481571.5:c.*180G>A | ENSP00000436597.1:n.*180G>A | |
| ENST00000483642.5:n.662G>A | ||
| ENST00000485484.5:n.531G>A | ||
| ENST00000488731.6:c.116-274G>A | ENSP00000432330.1:n.116-274G>A | |
| ENST00000492494.5:n.544G>A | ||
| ENST00000525160.5:c.*30-149G>A | ENSP00000431568.1:n.*30-149G>A | |
| ENST00000528013.6:c.409G>A | ENSP00000433130.2:p.Gly137Arg | |
| ENST00000529984.5:c.116-274G>A | ENSP00000437093.1:n.116-274G>A | |
| ENST00000531105.5:c.115+1283G>A | ENSP00000431292.1:n.115+1283G>A | |
| ENST00000533178.5:c.122-421G>A | ENSP00000436430.1:n.122-421G>A | |
| NM_001048171.1:c.409G>A | NP_001041636.1:p.Gly137Arg | |
| NM_001048172.1:c.370G>A | NP_001041637.1:p.Gly124Arg | |
| NM_001048173.1:c.367G>A | NP_001041638.1:p.Gly123Arg | |
| NM_001048174.1:c.367G>A | NP_001041639.1:p.Gly123Arg | |
| NM_001128425.1:c.451G>A , LRG_220t1:c.451G>A | NP_001121897.1:p.Gly151Arg | |
| NM_001293190.1:c.412G>A | NP_001280119.1:p.Gly138Arg | |
| NM_001293191.1:c.400G>A | NP_001280120.1:p.Gly134Arg | |
| NM_001293192.1:c.91G>A | NP_001280121.1:p.Gly31Arg | |
| NM_001293195.1:c.367G>A | NP_001280124.1:p.Gly123Arg | |
| NM_001293196.1:c.91G>A | NP_001280125.1:p.Gly31Arg | |
| NM_012222.2:c.442G>A | NP_036354.1:p.Gly148Arg | |
| XM_011541497.1:c.427G>A | XP_011539799.1:p.Gly143Arg | |
| XM_011541498.1:c.409G>A | XP_011539800.1:p.Gly137Arg | |
| XM_011541499.1:c.409G>A | XP_011539801.1:p.Gly137Arg | |
| XM_011541500.1:c.409G>A | XP_011539802.1:p.Gly137Arg | |
| XM_011541501.1:c.409G>A | XP_011539803.1:p.Gly137Arg | |
| XM_011541502.1:c.409G>A | XP_011539804.1:p.Gly137Arg | |
| XM_011541503.1:c.451G>A | XP_011539805.1:p.Gly151Arg | |
| XM_011541504.1:c.400G>A | XP_011539806.1:p.Gly134Arg | |
| XM_011541505.1:c.43-274G>A | XP_011539807.1:n.43-274G>A | |
| XM_011541506.1:c.43-274G>A | XP_011539808.1:n.43-274G>A | |
| XM_011541507.1:c.33+177G>A | XP_011539809.1:n.33+177G>A | |
| XM_011541508.1:c.7-149G>A | XP_011539810.1:n.7-149G>A | |
| XR_946658.1:n.498G>A | ||
| NM_001350650.1:c.34-149G>A | NP_001337579.1:n.34-149G>A | |
| NM_001350651.1:c.34-149G>A | NP_001337580.1:n.34-149G>A | |
| NR_146882.1:n.625G>A | ||
| NR_146883.1:n.451-149G>A | ||
| XM_011541497.3:c.427G>A | XP_011539799.1:p.Gly143Arg | |
| XM_011541500.3:c.409G>A | XP_011539802.1:p.Gly137Arg | |
| XM_011541501.2:c.409G>A | XP_011539803.1:p.Gly137Arg | |
| XM_011541502.2:c.409G>A | XP_011539804.1:p.Gly137Arg | |
| XM_011541503.2:c.451G>A | XP_011539805.1:p.Gly151Arg | |
| XM_011541504.2:c.400G>A | XP_011539806.1:p.Gly134Arg | |
| XM_011541505.2:c.43-274G>A | XP_011539807.1:n.43-274G>A | |
| XM_011541506.2:c.43-274G>A | XP_011539808.1:n.43-274G>A | |
| XM_017001331.1:c.409G>A | XP_016856820.1:p.Gly137Arg | |
| XM_017001332.1:c.409G>A | XP_016856821.1:p.Gly137Arg | |
| XM_017001333.1:c.409G>A | XP_016856822.1:p.Gly137Arg | |
| XM_017001334.1:c.370G>A | XP_016856823.1:p.Gly124Arg | |
| XM_017001335.1:c.91G>A | XP_016856824.1:p.Gly31Arg | |
| XM_017001336.1:c.34-149G>A | XP_016856825.1:n.34-149G>A | |
| XM_017001337.1:c.34-149G>A | XP_016856826.1:n.34-149G>A | |
| XM_024447244.1:c.34-149G>A | XP_024303012.1:n.34-149G>A | |
| XM_024447245.1:c.34-149G>A | XP_024303013.1:n.34-149G>A | |
| XM_024447248.1:c.33+177G>A | XP_024303016.1:n.33+177G>A | |
| XM_024447249.1:c.-287G>A | XP_024303017.1:n.-287G>A | |
| XM_024447250.1:c.-287G>A | XP_024303018.1:n.-287G>A | |
| XM_024447251.1:c.-221-149G>A | XP_024303019.1:n.-221-149G>A | |
| XR_001737190.1:n.412G>A | ||
| XR_001737192.1:n.277+177G>A | ||
| XR_002956643.1:n.457+177G>A | ||
| XR_002956644.1:n.719G>A | ||
| XR_946658.2:n.512G>A | ||
| NM_001048171.2:c.367G>A | NP_001041636.2:p.Gly123Arg | |
| NM_001128425.2:c.451G>A MANE Plus Clinical | NP_001121897.1:p.Gly151Arg | |
| NM_001048172.2:c.370G>A | NP_001041637.1:p.Gly124Arg | |
| NM_001048173.2:c.367G>A | NP_001041638.1:p.Gly123Arg | |
| NM_001048174.2:c.367G>A MANE Select | NP_001041639.1:p.Gly123Arg | |
| NM_001293190.2:c.412G>A | NP_001280119.1:p.Gly138Arg | |
| NM_001293191.2:c.400G>A | NP_001280120.1:p.Gly134Arg | |
| NM_001293192.2:c.91G>A | NP_001280121.1:p.Gly31Arg | |
| NM_001293195.2:c.367G>A | NP_001280124.1:p.Gly123Arg | |
| NM_001293196.2:c.91G>A | NP_001280125.1:p.Gly31Arg | |
| NM_001350650.2:c.34-149G>A | NP_001337579.1:n.34-149G>A | |
| NM_001350651.2:c.34-149G>A | NP_001337580.1:n.34-149G>A | |
| NM_012222.3:c.442G>A | NP_036354.1:p.Gly148Arg | |
| NR_146882.2:n.595G>A | ||
| NR_146883.2:n.456-149G>A |