Linked Data
ClinVar Variation Id:
30996
dbSNP Id:
rs202138550
ExAC:
17:8133261 G / A
gnomAD v2:
17-8133261-G-A
gnomAD v3:
17-8229943-G-A
gnomAD v4:
17-8229943-G-A
COSMIC:
COSM1387626
PubMed:
PMID:22267198
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8229943G>A , CM000679.2:g.8229943G>A | GRCh38 |
| NC_000017.10:g.8133261G>A , CM000679.1:g.8133261G>A | GRCh37 |
| NC_000017.9:g.8073986G>A | NCBI36 |
| NG_032148.1:g.23153C>T | |
| NG_032148.2:g.23153C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580299.2:c.2959C>T | ENSP00000462607.2:p.Arg987Trp | |
| ENST00000581729.2:c.2959C>T | ENSP00000462720.2:p.Arg987Trp | |
| ENST00000581967.2:n.3411C>T | ||
| ENST00000583254.2:n.4957C>T | ||
| ENST00000699849.1:c.2062C>T | ENSP00000514647.1:p.Arg688Trp | |
| ENST00000699850.1:n.2547C>T | ||
| ENST00000699851.1:n.3306C>T | ||
| ENST00000699852.1:c.*1537C>T | ENSP00000514648.1:n.*1537C>T | |
| ENST00000699853.1:c.2959C>T | ENSP00000514649.1:p.Arg987Trp | |
| ENST00000699854.1:n.3077C>T | ||
| ENST00000699855.1:n.3736C>T | ||
| ENST00000699856.1:c.2934-21C>T | ENSP00000514650.1:n.2934-21C>T | |
| ENST00000699857.1:n.3194C>T | ||
| ENST00000699858.1:c.*1897C>T | ENSP00000514651.1:n.*1897C>T | |
| ENST00000699859.1:c.2830C>T | ENSP00000514652.1:p.Arg944Trp | |
| ENST00000699860.1:n.1196C>T | ||
| ENST00000699861.1:n.2981C>T | ||
| ENST00000699862.1:n.4244C>T | ||
| ENST00000449476.7:c.2854C>T | ENSP00000396018.2:p.Arg952Trp | |
| ENST00000581671.2:n.2948C>T | ||
| ENST00000643543.1:c.*1666C>T | ENSP00000494323.1:n.*1666C>T | |
| ENST00000651323.1:c.2959C>T MANE Select | ENSP00000498499.1:p.Arg987Trp | |
| ENST00000315684.12:c.2959C>T | ENSP00000313759.8:p.Arg987Trp | |
| ENST00000449476.6:c.2854C>T | ENSP00000396018.2:p.Arg952Trp | |
| ENST00000578240.1:n.1512C>T | ||
| ENST00000578441.5:n.337-21C>T | ||
| ENST00000578537.1:c.636-21C>T | ||
| ENST00000580299.1:c.130C>T | ENSP00000462607.1:p.Arg44Trp | |
| NM_025099.5:c.2959C>T | NP_079375.3:p.Arg987Trp | |
| NR_046431.1:n.2913C>T | ||
| XM_006721577.2:c.2830C>T | XP_006721640.1:p.Arg944Trp | |
| XM_006721578.2:c.2959C>T | XP_006721641.1:p.Arg987Trp | |
| XM_006721579.2:c.2934-21C>T | XP_006721642.1:n.2934-21C>T | |
| XM_011524010.1:c.2854C>T | XP_011522312.1:p.Arg952Trp | |
| XM_011524011.1:c.2062C>T | XP_011522313.1:p.Arg688Trp | |
| XR_429823.2:n.3002C>T | ||
| XR_429824.2:n.3002C>T | ||
| XR_429825.1:n.2808C>T | ||
| NM_025099.6:c.2959C>T MANE Select | NP_079375.3:p.Arg987Trp | |
| XM_006721577.3:c.2830C>T | XP_006721640.1:p.Arg944Trp | |
| XM_006721578.3:c.2959C>T | XP_006721641.1:p.Arg987Trp | |
| XM_011524010.2:c.2854C>T | XP_011522312.1:p.Arg952Trp | |
| XM_011524011.2:c.2062C>T | XP_011522313.1:p.Arg688Trp | |
| XR_001752639.1:n.2873C>T | ||
| XR_001752640.1:n.2977-21C>T | ||
| XR_001752641.1:n.2977-21C>T | ||
| XR_001752642.1:n.2808C>T | ||
| XR_001752643.1:n.3432C>T | ||
| XR_002958073.1:n.2808C>T | ||
| XR_429823.3:n.3002C>T | ||
| XR_429824.3:n.3002C>T | ||
| NR_046431.2:n.2874C>T |