Linked Data
ClinVar Variation Id:
1776
ClinVar RCV Id:
RCV002508755
dbSNP Id:
rs121918335
PubMed:
PMID:19780765
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.792340C>A , CM000673.2:g.792340C>A | GRCh38 |
| NC_000011.9:g.792340C>A , CM000673.1:g.792340C>A | GRCh37 |
| NC_000011.8:g.782340C>A | NCBI36 |
| NG_023407.1:g.10930G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000628067.3:c.706G>T MANE Select | ENSP00000486058.1:p.Gly236Trp | |
| ENST00000320230.9:c.706G>T | ENSP00000322020.5:p.Gly236Trp | |
| ENST00000481290.5:c.781G>T | ENSP00000431829.2:p.Gly261Trp | |
| ENST00000531214.5:c.706G>T | ENSP00000437236.1:p.Gly236Trp | |
| ENST00000627843.2:c.706G>T | ENSP00000486512.1:p.Gly236Trp | |
| ENST00000628067.2:c.706G>T | ENSP00000486058.1:p.Gly236Trp | |
| NM_001191060.1:c.706G>T | NP_001177989.1:p.Gly236Trp | |
| NM_001191061.1:c.706G>T | NP_001177990.1:p.Gly236Trp | |
| NM_024698.5:c.706G>T | NP_078974.1:p.Gly236Trp | |
| XM_011520369.1:c.706G>T | XP_011518671.1:p.Gly236Trp | |
| XM_011520370.1:c.706G>T | XP_011518672.1:p.Gly236Trp | |
| XM_011520371.1:c.706G>T | XP_011518673.1:p.Gly236Trp | |
| XM_011520370.2:c.706G>T | XP_011518672.1:p.Gly236Trp | |
| XM_011520371.2:c.706G>T | XP_011518673.1:p.Gly236Trp | |
| XM_024448687.1:c.706G>T | XP_024304455.1:p.Gly236Trp | |
| XM_024448688.1:c.706G>T | XP_024304456.1:p.Gly236Trp | |
| XM_024448689.1:c.706G>T | XP_024304457.1:p.Gly236Trp | |
| NM_001191061.2:c.706G>T MANE Select | NP_001177990.1:p.Gly236Trp | |
| NM_024698.6:c.706G>T | NP_078974.1:p.Gly236Trp | |
| NM_001191060.2:c.706G>T | NP_001177989.1:p.Gly236Trp |