Linked Data
dbSNP Id:
rs757670960
ExAC:
11:118963139 C / T
gnomAD v2:
11-118963139-C-T
gnomAD v4:
11-119092429-C-T
COSMIC:
COSM6014696
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119092429C>T , CM000673.2:g.119092429C>T | GRCh38 |
| NC_000011.9:g.118963139C>T , CM000673.1:g.118963139C>T | GRCh37 |
| NC_000011.8:g.118468349C>T | NCBI36 |
| NG_008093.1:g.12553C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000686218.1:c.512C>T | ENSP00000509288.1:p.Ala171Val | |
| ENST00000691144.1:n.2658C>T | ||
| ENST00000691249.1:n.1501C>T | ||
| ENST00000442944.7:c.659C>T | ENSP00000392041.3:p.Ala220Val | |
| ENST00000536813.6:c.626C>T | ENSP00000438726.2:p.Ala209Val | |
| ENST00000640813.1:c.487C>T | ENSP00000491061.1:p.Pro163Ser | |
| ENST00000648026.1:c.571C>T | ENSP00000498044.1:p.Pro191Ser | |
| ENST00000648374.1:c.626C>T | ENSP00000497255.1:p.Ala209Val | |
| ENST00000649823.1:n.1134C>T | ||
| ENST00000650101.1:c.608C>T | ENSP00000496970.1:p.Ala203Val | |
| ENST00000650307.1:n.1503C>T | ||
| ENST00000652429.1:c.677C>T MANE Select | ENSP00000498786.1:p.Ala226Val | |
| ENST00000278715.7:c.677C>T | ENSP00000278715.3:p.Ala226Val | |
| ENST00000392841.1:c.626C>T | ENSP00000376584.1:p.Ala209Val | |
| ENST00000442944.6:c.626C>T | ENSP00000392041.2:p.Ala209Val | |
| ENST00000537841.5:c.626C>T | ENSP00000444730.1:p.Ala209Val | |
| ENST00000542044.5:n.1122C>T | ||
| ENST00000542729.5:c.600+266C>T | ENSP00000443058.1:n.600+266C>T | |
| ENST00000543090.5:c.584C>T | ENSP00000445429.1:p.Ala195Val | |
| ENST00000543543.5:n.1152C>T | ||
| ENST00000544182.1:n.892C>T | ||
| ENST00000544387.5:c.651+266C>T | ENSP00000438424.1:n.651+266C>T | |
| ENST00000545621.5:c.*812C>T | ENSP00000444849.1:n.*812C>T | |
| ENST00000546226.5:n.1205C>T | ||
| NM_000190.3:c.677C>T | NP_000181.2:p.Ala226Val | |
| NM_001024382.1:c.626C>T | NP_001019553.1:p.Ala209Val | |
| NM_001258208.1:c.651+266C>T | NP_001245137.1:n.651+266C>T | |
| NM_001258209.1:c.600+266C>T | NP_001245138.1:n.600+266C>T | |
| XM_005271531.1:c.626C>T | XP_005271588.1:p.Ala209Val | |
| XM_005271532.1:c.626C>T | XP_005271589.1:p.Ala209Val | |
| XM_005271533.2:c.623C>T | XP_005271590.1:p.Ala208Val | |
| XM_011542796.1:c.512C>T | XP_011541098.1:p.Ala171Val | |
| NM_000190.4:c.677C>T MANE Select | NP_000181.2:p.Ala226Val | |
| NM_001024382.2:c.626C>T | NP_001019553.1:p.Ala209Val | |
| XM_005271533.3:c.623C>T | XP_005271590.1:p.Ala208Val | |
| XM_017017629.1:c.626C>T | XP_016873118.1:p.Ala209Val | |
| XM_024448460.1:c.597+266C>T | XP_024304228.1:n.597+266C>T | |
| NM_001258208.2:c.651+266C>T | NP_001245137.1:n.651+266C>T | |
| NM_001258209.2:c.600+266C>T | NP_001245138.1:n.600+266C>T |