Canonical Allele Identifier: CA544751947

Gene: PROS1

Linked Data

• dbSNP Id: rs1319867630
• gnomAD v2: 3-93624602-T-C
• gnomAD v4: 3-93905758-T-C
• MyVariant Identifiers: chr3:g.93624602T>C (hg19) ; chr3:g.93905758T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905758T>C , CM000665.2:g.93905758T>C	GRCh38
NC_000003.11:g.93624602T>C , CM000665.1:g.93624602T>C	GRCh37
NC_000003.10:g.95107292T>C	NCBI36
NG_009813.1:g.73333A>G , LRG_572:g.73333A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.601+26A>G	ENSP00000330021.7:n.601+26A>G
ENST00000394236.9:c.601+26A>G MANE Select	ENSP00000377783.3:n.601+26A>G
ENST00000407433.6:c.556+71A>G	ENSP00000385794.2:n.556+71A>G
ENST00000647936.1:c.601+26A>G	ENSP00000496822.1:n.601+26A>G
ENST00000648381.1:n.769+26A>G
ENST00000648853.1:c.559+26A>G	ENSP00000497262.1:n.559+26A>G
ENST00000649103.1:c.700+26A>G	ENSP00000497962.1:n.700+26A>G
ENST00000650591.1:c.697+26A>G	ENSP00000497376.1:n.697+26A>G
ENST00000394236.7:c.601+26A>G	ENSP00000377783.3:n.601+26A>G
ENST00000407433.5:c.208+26A>G	ENSP00000385794.1:n.208+26A>G
NM_000313.3:c.601+26A>G , LRG_572t1:c.601+26A>G	NP_000304.2:n.601+26A>G
NM_001314077.1:c.697+26A>G , LRG_572t2:c.697+26A>G	NP_001301006.1:n.697+26A>G
NM_000313.4:c.601+26A>G MANE Select	NP_000304.2:n.601+26A>G
NM_001314077.2:c.697+26A>G	NP_001301006.1:n.697+26A>G