Linked Data
ClinVar Variation Id:
16465
ClinVar RCV Id:
RCV000017929
dbSNP Id:
rs137854484
PubMed:
PMID:17366579
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48488193C>T , CM000677.2:g.48488193C>T | GRCh38 |
| NC_000015.9:g.48780390C>T , CM000677.1:g.48780390C>T | GRCh37 |
| NC_000015.8:g.46567682C>T | NCBI36 |
| NG_008805.2:g.162596G>A , LRG_778:g.162596G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000559133.6:c.3257G>A | ENSP00000453958.2:p.Cys1086Tyr | |
| ENST00000674301.2:c.3257G>A | ENSP00000501333.2:p.Cys1086Tyr | |
| ENST00000684448.1:n.1931G>A | ||
| ENST00000316623.10:c.3257G>A MANE Select | ENSP00000325527.5:p.Cys1086Tyr | |
| ENST00000316623.9:c.3257G>A | ENSP00000325527.5:p.Cys1086Tyr | |
| ENST00000537463.6:c.637-13543G>A | ENSP00000440294.2:n.637-13543G>A | |
| NM_000138.4:c.3257G>A , LRG_778t1:c.3257G>A | NP_000129.3:p.Cys1086Tyr | |
| NM_000138.5:c.3257G>A MANE Select | NP_000129.3:p.Cys1086Tyr |