Canonical Allele Identifier: CA78492921
Gene: PROS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4857037

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93908968G>A , CM000665.2:g.93908968G>A GRCh38
NC_000003.11:g.93627812G>A , CM000665.1:g.93627812G>A GRCh37
NC_000003.10:g.95110502G>A NCBI36
NG_009813.1:g.70123C>T , LRG_572:g.70123C>T

Transcript Alleles

HGVS Amino-acid change
NM_000313.3:c.346+1651C>T , LRG_572t1:c.346+1651C>T NP_000304.2:p.=
NM_001314077.1:c.442+1651C>T , LRG_572t2:c.442+1651C>T NP_001301006.1:p.=
ENST00000348974.4:c.442+1651C>T ENSP00000330021.6:p.=
ENST00000394236.7:c.346+1651C>T ENSP00000377783.3:p.=
ENST00000407433.5:c.-48+1651C>T ENSP00000385794.1:p.=
ENST00000472684.1:c.-48+1651C>T ENSP00000419616.1:p.=
ENST00000488658.1:n.539+1651C>T