Linked Data
ClinVar Variation Id:
156452
ClinVar RCV Id:
RCV000144512
dbSNP Id:
rs587777796
PubMed:
PMID:23246288
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.179219719T>G , CM000665.2:g.179219719T>G | GRCh38 |
| NC_000003.11:g.178937507T>G , CM000665.1:g.178937507T>G | GRCh37 |
| NC_000003.10:g.180420201T>G | NCBI36 |
| NG_012113.2:g.76197T>G , LRG_310:g.76197T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263967.4:c.1895T>G MANE Select | ENSP00000263967.3:p.Leu632Ter | |
| ENST00000462255.2:n.357T>G | ||
| ENST00000643187.1:c.1895T>G | ENSP00000493507.1:p.Leu632Ter | |
| ENST00000674534.1:n.2803T>G | ||
| ENST00000674622.1:c.316T>G | ENSP00000502417.1:n.316T>G | |
| ENST00000675467.1:n.4702T>G | ||
| ENST00000675786.1:c.*462T>G | ENSP00000502323.1:n.*462T>G | |
| ENST00000263967.3:c.1895T>G | ENSP00000263967.3:p.Leu632Ter | |
| ENST00000462255.1:n.169T>G | ||
| NM_006218.2:c.1895T>G , LRG_310t1:c.1895T>G | NP_006209.2:p.Leu632Ter | |
| XM_006713658.2:c.1895T>G | XP_006713721.1:p.Leu632Ter | |
| XM_011512894.1:c.1895T>G | XP_011511196.1:p.Leu632Ter | |
| NM_006218.3:c.1895T>G | NP_006209.2:p.Leu632Ter | |
| XM_006713658.4:c.1895T>G | XP_006713721.1:p.Leu632Ter | |
| XM_011512894.2:c.1895T>G | XP_011511196.1:p.Leu632Ter | |
| NM_006218.4:c.1895T>G MANE Select | NP_006209.2:p.Leu632Ter |