Canonical Allele Identifier: CA78520076

Gene: PROS1

Linked Data

• dbSNP Id: rs896036595
• gnomAD v3: 3-93874147-C-A
• gnomAD v4: 3-93874147-C-A
• MyVariant Identifiers: chr3:g.93592991C>A (hg19) ; chr3:g.93874147C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874147C>A , CM000665.2:g.93874147C>A	GRCh38
NC_000003.11:g.93592991C>A , CM000665.1:g.93592991C>A	GRCh37
NC_000003.10:g.95075681C>A	NCBI36
NG_009813.1:g.104944G>T , LRG_572:g.104944G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.*1+97G>T	ENSP00000330021.7:n.*1+97G>T
ENST00000394236.9:c.*98G>T MANE Select	ENSP00000377783.3:n.*98G>T
ENST00000407433.6:c.*98G>T	ENSP00000385794.2:n.*98G>T
ENST00000647936.1:c.*232G>T	ENSP00000496822.1:n.*232G>T
ENST00000648381.1:n.2297G>T
ENST00000648853.1:c.*98G>T	ENSP00000497262.1:n.*98G>T
ENST00000650591.1:c.*98G>T	ENSP00000497376.1:n.*98G>T
ENST00000394236.7:c.*98G>T	ENSP00000377783.3:n.*98G>T
ENST00000407433.5:c.*98G>T	ENSP00000385794.1:n.*98G>T
NM_000313.3:c.*98G>T , LRG_572t1:c.*98G>T	NP_000304.2:n.*98G>T
NM_001314077.1:c.*98G>T , LRG_572t2:c.*98G>T	NP_001301006.1:n.*98G>T
NM_000313.4:c.*98G>T MANE Select	NP_000304.2:n.*98G>T
NM_001314077.2:c.*98G>T	NP_001301006.1:n.*98G>T