Linked Data
ClinVar Variation Id:
200005
dbSNP Id:
rs112911555
gnomAD v2:
15-48782269-C-T
gnomAD v4:
15-48490072-C-T
PubMed:
PMID:19159394
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48490072C>T , CM000677.2:g.48490072C>T | GRCh38 |
| NC_000015.9:g.48782269C>T , CM000677.1:g.48782269C>T | GRCh37 |
| NC_000015.8:g.46569561C>T | NCBI36 |
| NG_008805.2:g.160717G>A , LRG_778:g.160717G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.2861G>A | ENSP00000453958.2:p.Arg954His | |
| ENST00000674301.2:c.2861G>A | ENSP00000501333.2:p.Arg954His | |
| ENST00000684448.1:n.1535G>A | ||
| ENST00000316623.10:c.2861G>A MANE Select | ENSP00000325527.5:p.Arg954His | |
| ENST00000316623.9:c.2861G>A | ENSP00000325527.5:p.Arg954His | |
| ENST00000537463.6:c.637-15422G>A | ENSP00000440294.2:n.637-15422G>A | |
| NM_000138.4:c.2861G>A , LRG_778t1:c.2861G>A | NP_000129.3:p.Arg954His | |
| NM_000138.5:c.2861G>A MANE Select | NP_000129.3:p.Arg954His |