Linked Data
ClinVar Variation Id:
13871
ClinVar RCV Id:
RCV000014885
dbSNP Id:
rs267606827
PubMed:
PMID:19564653
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28768203G>A , CM000676.2:g.28768203G>A | GRCh38 |
| NC_000014.8:g.29237409G>A , CM000676.1:g.29237409G>A | GRCh37 |
| NC_000014.7:g.28307160G>A | NCBI36 |
| NG_009367.1:g.6123G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706482.1:c.924G>A | ENSP00000516406.1:p.Trp308Ter | |
| ENST00000313071.7:c.924G>A MANE Select | ENSP00000339004.3:p.Trp308Ter | |
| ENST00000313071.6:c.924G>A | ENSP00000339004.3:p.Trp308Ter | |
| NM_005249.4:c.924G>A | NP_005240.3:p.Trp308Ter | |
| NM_005249.5:c.924G>A MANE Select | NP_005240.3:p.Trp308Ter |