Linked Data
dbSNP Id:
rs1200534030
gnomAD v2:
11-118963943-G-A
gnomAD v3:
11-119093233-G-A
gnomAD v4:
11-119093233-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119093233G>A , CM000673.2:g.119093233G>A | GRCh38 |
| NC_000011.9:g.118963943G>A , CM000673.1:g.118963943G>A | GRCh37 |
| NC_000011.8:g.118469153G>A | NCBI36 |
| NG_008093.1:g.13357G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686218.1:c.871G>A | ENSP00000509288.1:p.Gly291Arg | |
| ENST00000691144.1:n.3251G>A | ||
| ENST00000691249.1:n.1860G>A | ||
| ENST00000442944.7:c.1018G>A | ENSP00000392041.3:p.Gly340Arg | |
| ENST00000640813.1:c.*273G>A | ENSP00000491061.1:n.*273G>A | |
| ENST00000648026.1:c.930G>A | ENSP00000498044.1:n.930G>A | |
| ENST00000648374.1:c.985G>A | ENSP00000497255.1:p.Gly329Arg | |
| ENST00000650101.1:c.967G>A | ENSP00000496970.1:p.Gly323Arg | |
| ENST00000650307.1:n.1862G>A | ||
| ENST00000652429.1:c.1036G>A MANE Select | ENSP00000498786.1:p.Gly346Arg | |
| ENST00000278715.7:c.1036G>A | ENSP00000278715.3:p.Gly346Arg | |
| ENST00000392841.1:c.985G>A | ENSP00000376584.1:p.Gly329Arg | |
| ENST00000442944.6:c.985G>A | ENSP00000392041.2:p.Gly329Arg | |
| ENST00000537841.5:c.985G>A | ENSP00000444730.1:p.Gly329Arg | |
| ENST00000539045.1:n.535G>A | ||
| ENST00000542044.5:n.1481G>A | ||
| ENST00000542729.5:c.865G>A | ENSP00000443058.1:p.Gly289Arg | |
| ENST00000543090.5:c.943G>A | ENSP00000445429.1:p.Gly315Arg | |
| ENST00000543543.5:n.1511G>A | ||
| ENST00000544182.1:n.1485G>A | ||
| ENST00000544387.5:c.916G>A | ENSP00000438424.1:p.Gly306Arg | |
| ENST00000546226.5:n.1798G>A | ||
| NM_000190.3:c.1036G>A | NP_000181.2:p.Gly346Arg | |
| NM_001024382.1:c.985G>A | NP_001019553.1:p.Gly329Arg | |
| NM_001258208.1:c.916G>A | NP_001245137.1:p.Gly306Arg | |
| NM_001258209.1:c.865G>A | NP_001245138.1:p.Gly289Arg | |
| XM_005271531.1:c.985G>A | XP_005271588.1:p.Gly329Arg | |
| XM_005271532.1:c.985G>A | XP_005271589.1:p.Gly329Arg | |
| XM_005271533.2:c.982G>A | XP_005271590.1:p.Gly328Arg | |
| XM_011542796.1:c.871G>A | XP_011541098.1:p.Gly291Arg | |
| NM_000190.4:c.1036G>A MANE Select | NP_000181.2:p.Gly346Arg | |
| NM_001024382.2:c.985G>A | NP_001019553.1:p.Gly329Arg | |
| XM_005271533.3:c.982G>A | XP_005271590.1:p.Gly328Arg | |
| XM_017017629.1:c.985G>A | XP_016873118.1:p.Gly329Arg | |
| XM_024448460.1:c.862G>A | XP_024304228.1:p.Gly288Arg | |
| NM_001258208.2:c.916G>A | NP_001245137.1:p.Gly306Arg | |
| NM_001258209.2:c.865G>A | NP_001245138.1:p.Gly289Arg |