Linked Data
ClinVar Variation Id:
13824
ClinVar RCV Id:
RCV000014835
dbSNP Id:
rs121917712
COSMIC:
COSM1450731
PubMed:
PMID:12794692
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41972567G>A , CM000669.2:g.41972567G>A | GRCh38 |
| NC_000007.13:g.42012166G>A , CM000669.1:g.42012166G>A | GRCh37 |
| NC_000007.12:g.41978691G>A | NCBI36 |
| NG_008434.1:g.269453C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395925.8:c.1873C>T MANE Select | ENSP00000379258.3:p.Arg625Trp | |
| ENST00000677288.1:c.1699C>T | ENSP00000503986.1:p.Arg567Trp | |
| ENST00000677605.1:c.1873C>T | ENSP00000503743.1:p.Arg625Trp | |
| ENST00000678429.1:c.1873C>T | ENSP00000502957.1:p.Arg625Trp | |
| ENST00000395925.7:c.1873C>T | ENSP00000379258.3:p.Arg625Trp | |
| ENST00000464291.1:n.426C>T | ||
| ENST00000479210.1:n.1850C>T | ||
| NM_000168.5:c.1873C>T | NP_000159.3:p.Arg625Trp | |
| XM_005249703.1:c.1873C>T | XP_005249760.1:p.Arg625Trp | |
| XM_005249704.2:c.1873C>T | XP_005249761.1:p.Arg625Trp | |
| XM_011515272.1:c.1873C>T | XP_011513574.1:p.Arg625Trp | |
| XM_011515273.1:c.1873C>T | XP_011513575.1:p.Arg625Trp | |
| XM_011515274.1:c.1696C>T | XP_011513576.1:p.Arg566Trp | |
| XM_011515274.2:c.1696C>T | XP_011513576.1:p.Arg566Trp | |
| XM_017011997.1:c.1870C>T | XP_016867486.1:p.Arg624Trp | |
| NM_000168.6:c.1873C>T MANE Select | NP_000159.3:p.Arg625Trp |