Linked Data
ClinVar Variation Id:
13494
ClinVar RCV Id:
RCV000014438
dbSNP Id:
rs121918067
PubMed:
PMID:19903818
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912141A>G , CM000674.2:g.4912141A>G | GRCh38 |
| NC_000012.11:g.5021307A>G , CM000674.1:g.5021307A>G | GRCh37 |
| NC_000012.10:g.4891568A>G | NCBI36 |
| NG_011815.1:g.7235A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382545.5:c.763A>G MANE Select | ENSP00000371985.3:p.Asn255Asp | |
| ENST00000543874.3:n.105+1669A>G | ||
| ENST00000639306.1:c.601A>G | ENSP00000492506.1:p.Asn201Asp | |
| ENST00000382545.3:c.763A>G | ENSP00000371985.3:p.Asn255Asp | |
| ENST00000541095.1:n.105+1669A>G | ||
| ENST00000543874.2:n.96+1669A>G | ||
| NM_000217.2:c.763A>G | NP_000208.2:p.Asn255Asp | |
| NM_000217.3:c.763A>G MANE Select | NP_000208.2:p.Asn255Asp |