Canonical Allele Identifier: CA123035
Gene: PROS1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13322
ClinVar RCV Id: RCV000014250
dbSNP Id: rs121918475

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93898462G>A , CM000665.2:g.93898462G>A GRCh38
NC_000003.11:g.93617306G>A , CM000665.1:g.93617306G>A GRCh37
NC_000003.10:g.95099996G>A NCBI36
NG_009813.1:g.80629C>T , LRG_572:g.80629C>T

Transcript Alleles

HGVS Amino-acid change
NM_000313.3:c.835C>T , LRG_572t1:c.835C>T NP_000304.2:p.Gln279Ter
NM_001314077.1:c.931C>T , LRG_572t2:c.931C>T NP_001301006.1:p.Gln311Ter
ENST00000394236.7:c.835C>T ENSP00000377783.3:p.Gln279Ter
ENST00000407433.5:c.442C>T ENSP00000385794.1:p.Gln148Ter