Canonical Allele Identifier: CA78520079

Gene: PROS1

Linked Data

• dbSNP Id: rs553753206
• gnomAD v3: 3-93874149-A-G
• gnomAD v4: 3-93874149-A-G
• MyVariant Identifiers: chr3:g.93592993A>G (hg19) ; chr3:g.93874149A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874149A>G , CM000665.2:g.93874149A>G	GRCh38
NC_000003.11:g.93592993A>G , CM000665.1:g.93592993A>G	GRCh37
NC_000003.10:g.95075683A>G	NCBI36
NG_009813.1:g.104942T>C , LRG_572:g.104942T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.*1+95T>C	ENSP00000330021.7:n.*1+95T>C
ENST00000394236.9:c.*96T>C MANE Select	ENSP00000377783.3:n.*96T>C
ENST00000407433.6:c.*96T>C	ENSP00000385794.2:n.*96T>C
ENST00000647936.1:c.*230T>C	ENSP00000496822.1:n.*230T>C
ENST00000648381.1:n.2295T>C
ENST00000648853.1:c.*96T>C	ENSP00000497262.1:n.*96T>C
ENST00000650591.1:c.*96T>C	ENSP00000497376.1:n.*96T>C
ENST00000394236.7:c.*96T>C	ENSP00000377783.3:n.*96T>C
ENST00000407433.5:c.*96T>C	ENSP00000385794.1:n.*96T>C
NM_000313.3:c.*96T>C , LRG_572t1:c.*96T>C	NP_000304.2:n.*96T>C
NM_001314077.1:c.*96T>C , LRG_572t2:c.*96T>C	NP_001301006.1:n.*96T>C
NM_000313.4:c.*96T>C MANE Select	NP_000304.2:n.*96T>C
NM_001314077.2:c.*96T>C	NP_001301006.1:n.*96T>C