Linked Data
ClinVar Variation Id:
135740
ClinVar RCV Id:
RCV000122829
RCV000123724
RCV000211971
RCV000586136
RCV001798389
RCV003315804
RCV001356414
dbSNP Id:
rs1800055
ExAC:
11:108124628 T / C
gnomAD v2:
11-108124628-T-C
gnomAD v3:
11-108253901-T-C
gnomAD v4:
11-108253901-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108253901T>C , CM000673.2:g.108253901T>C | GRCh38 |
| NC_000011.9:g.108124628T>C , CM000673.1:g.108124628T>C | GRCh37 |
| NC_000011.8:g.107629838T>C | NCBI36 |
| NG_009830.1:g.36070T>C , LRG_135:g.36070T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.1986T>C | ENSP00000388058.2:p.Phe662= | |
| ENST00000713593.1:c.*1457T>C | ENSP00000518889.1:n.*1457T>C | |
| ENST00000278616.9:c.1986T>C | ENSP00000278616.4:p.Phe662= | |
| ENST00000682516.1:n.2120T>C | ||
| ENST00000683174.1:n.2136T>C | ||
| ENST00000683605.1:n.1481T>C | ||
| ENST00000684037.1:c.*921T>C | ENSP00000508245.1:n.*921T>C | |
| ENST00000684061.1:n.2120T>C | ||
| ENST00000527805.6:c.1986T>C | ENSP00000435747.2:p.Phe662= | |
| ENST00000675595.1:c.1821T>C | ENSP00000502563.1:p.Phe607= | |
| ENST00000675843.1:c.1986T>C MANE Select | ENSP00000501606.1:p.Phe662= | |
| ENST00000278616.8:c.1986T>C | ENSP00000278616.4:p.Phe662= | |
| ENST00000452508.6:c.1986T>C | ENSP00000388058.2:p.Phe662= | |
| ENST00000525012.5:n.163T>C | ||
| ENST00000527805.5:c.1986T>C | ENSP00000435747.1:p.Phe662= | |
| ENST00000533526.1:n.139T>C | ||
| NM_000051.3:c.1986T>C , LRG_135t1:c.1986T>C | NP_000042.3:p.Phe662= | |
| XM_005271561.3:c.1986T>C | XP_005271618.2:p.Phe662= | |
| XM_005271562.3:c.1986T>C | XP_005271619.2:p.Phe662= | |
| XM_006718843.2:c.1986T>C | XP_006718906.1:p.Phe662= | |
| XM_011542840.1:c.1986T>C | XP_011541142.1:p.Phe662= | |
| XM_011542841.1:c.1986T>C | XP_011541143.1:p.Phe662= | |
| XM_011542842.1:c.1821T>C | XP_011541144.1:p.Phe607= | |
| XM_011542843.1:c.1986T>C | XP_011541145.1:p.Phe662= | |
| XM_011542844.1:c.942T>C | XP_011541146.1:p.Phe314= | |
| XM_011542845.1:c.678T>C | XP_011541147.1:p.Phe226= | |
| XM_011542846.1:c.1986T>C | XP_011541148.1:p.Phe662= | |
| NM_001351834.1:c.1986T>C | NP_001338763.1:p.Phe662= | |
| XM_005271562.5:c.1986T>C | XP_005271619.2:p.Phe662= | |
| XM_006718843.4:c.1986T>C | XP_006718906.1:p.Phe662= | |
| XM_011542840.3:c.1986T>C | XP_011541142.1:p.Phe662= | |
| XM_011542842.3:c.1821T>C | XP_011541144.1:p.Phe607= | |
| XM_011542843.2:c.1986T>C | XP_011541145.1:p.Phe662= | |
| XM_011542844.3:c.942T>C | XP_011541146.1:p.Phe314= | |
| XM_011542845.2:c.678T>C | XP_011541147.1:p.Phe226= | |
| XM_017017789.2:c.1986T>C | XP_016873278.1:p.Phe662= | |
| XM_017017790.2:c.1986T>C | XP_016873279.1:p.Phe662= | |
| XM_017017791.1:c.1986T>C | XP_016873280.1:p.Phe662= | |
| XM_017017792.2:c.1986T>C | XP_016873281.1:p.Phe662= | |
| XR_002957150.1:n.2719T>C | ||
| NM_001351834.2:c.1986T>C | NP_001338763.1:p.Phe662= | |
| NM_000051.4:c.1986T>C MANE Select | NP_000042.3:p.Phe662= |