Linked Data
ClinVar Variation Id:
127339
ClinVar RCV Id:
RCV000115143
RCV000211963
RCV000168231
RCV000515225
RCV003237336
RCV001818258
RCV004549539
RCV003149791
dbSNP Id:
rs587779816
ExAC:
11:108121708 G / T
gnomAD v2:
11-108121708-G-T
gnomAD v3:
11-108250981-G-T
gnomAD v4:
11-108250981-G-T
PubMed:
PMID:25318351
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108250981G>T , CM000673.2:g.108250981G>T | GRCh38 |
| NC_000011.9:g.108121708G>T , CM000673.1:g.108121708G>T | GRCh37 |
| NC_000011.8:g.107626918G>T | NCBI36 |
| NG_009830.1:g.33150G>T , LRG_135:g.33150G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.1516G>T | ENSP00000388058.2:p.Gly506Cys | |
| ENST00000713593.1:c.*987G>T | ENSP00000518889.1:n.*987G>T | |
| ENST00000278616.9:c.1516G>T | ENSP00000278616.4:p.Gly506Cys | |
| ENST00000682516.1:n.1650G>T | ||
| ENST00000682956.1:n.1650G>T | ||
| ENST00000683174.1:n.1666G>T | ||
| ENST00000683605.1:n.1011G>T | ||
| ENST00000684037.1:c.*451G>T | ENSP00000508245.1:n.*451G>T | |
| ENST00000684061.1:n.1650G>T | ||
| ENST00000684179.1:n.1485G>T | ||
| ENST00000527805.6:c.1516G>T | ENSP00000435747.2:p.Gly506Cys | |
| ENST00000675595.1:c.1351G>T | ENSP00000502563.1:p.Gly451Cys | |
| ENST00000675843.1:c.1516G>T MANE Select | ENSP00000501606.1:p.Gly506Cys | |
| ENST00000278616.8:c.1516G>T | ENSP00000278616.4:p.Gly506Cys | |
| ENST00000452508.6:c.1516G>T | ENSP00000388058.2:p.Gly506Cys | |
| ENST00000527805.5:c.1516G>T | ENSP00000435747.1:p.Gly506Cys | |
| NM_000051.3:c.1516G>T , LRG_135t1:c.1516G>T | NP_000042.3:p.Gly506Cys | |
| XM_005271561.3:c.1516G>T | XP_005271618.2:p.Gly506Cys | |
| XM_005271562.3:c.1516G>T | XP_005271619.2:p.Gly506Cys | |
| XM_006718843.2:c.1516G>T | XP_006718906.1:p.Gly506Cys | |
| XM_011542840.1:c.1516G>T | XP_011541142.1:p.Gly506Cys | |
| XM_011542841.1:c.1516G>T | XP_011541143.1:p.Gly506Cys | |
| XM_011542842.1:c.1351G>T | XP_011541144.1:p.Gly451Cys | |
| XM_011542843.1:c.1516G>T | XP_011541145.1:p.Gly506Cys | |
| XM_011542844.1:c.472G>T | XP_011541146.1:p.Gly158Cys | |
| XM_011542845.1:c.208G>T | XP_011541147.1:p.Gly70Cys | |
| XM_011542846.1:c.1516G>T | XP_011541148.1:p.Gly506Cys | |
| NM_001351834.1:c.1516G>T | NP_001338763.1:p.Gly506Cys | |
| XM_005271562.5:c.1516G>T | XP_005271619.2:p.Gly506Cys | |
| XM_006718843.4:c.1516G>T | XP_006718906.1:p.Gly506Cys | |
| XM_011542840.3:c.1516G>T | XP_011541142.1:p.Gly506Cys | |
| XM_011542842.3:c.1351G>T | XP_011541144.1:p.Gly451Cys | |
| XM_011542843.2:c.1516G>T | XP_011541145.1:p.Gly506Cys | |
| XM_011542844.3:c.472G>T | XP_011541146.1:p.Gly158Cys | |
| XM_011542845.2:c.208G>T | XP_011541147.1:p.Gly70Cys | |
| XM_017017789.2:c.1516G>T | XP_016873278.1:p.Gly506Cys | |
| XM_017017790.2:c.1516G>T | XP_016873279.1:p.Gly506Cys | |
| XM_017017791.1:c.1516G>T | XP_016873280.1:p.Gly506Cys | |
| XM_017017792.2:c.1516G>T | XP_016873281.1:p.Gly506Cys | |
| XR_002957150.1:n.2249G>T | ||
| NM_001351834.2:c.1516G>T | NP_001338763.1:p.Gly506Cys | |
| NM_000051.4:c.1516G>T MANE Select | NP_000042.3:p.Gly506Cys |