Canonical Allele Identifier: CA912655595

Gene: PROS1

Linked Data

• dbSNP Id: rs1341265416
• MyVariant Identifiers: chr3:g.93624596A>G (hg19) ; chr3:g.93905752A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905752A>G , CM000665.2:g.93905752A>G	GRCh38
NC_000003.11:g.93624596A>G , CM000665.1:g.93624596A>G	GRCh37
NC_000003.10:g.95107286A>G	NCBI36
NG_009813.1:g.73339T>C , LRG_572:g.73339T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.601+32T>C	ENSP00000330021.7:n.601+32T>C
ENST00000394236.9:c.601+32T>C MANE Select	ENSP00000377783.3:n.601+32T>C
ENST00000407433.6:c.556+77T>C	ENSP00000385794.2:n.556+77T>C
ENST00000647936.1:c.601+32T>C	ENSP00000496822.1:n.601+32T>C
ENST00000648381.1:n.769+32T>C
ENST00000648853.1:c.559+32T>C	ENSP00000497262.1:n.559+32T>C
ENST00000649103.1:c.700+32T>C	ENSP00000497962.1:n.700+32T>C
ENST00000650591.1:c.697+32T>C	ENSP00000497376.1:n.697+32T>C
ENST00000394236.7:c.601+32T>C	ENSP00000377783.3:n.601+32T>C
ENST00000407433.5:c.208+32T>C	ENSP00000385794.1:n.208+32T>C
NM_000313.3:c.601+32T>C , LRG_572t1:c.601+32T>C	NP_000304.2:n.601+32T>C
NM_001314077.1:c.697+32T>C , LRG_572t2:c.697+32T>C	NP_001301006.1:n.697+32T>C
NM_000313.4:c.601+32T>C MANE Select	NP_000304.2:n.601+32T>C
NM_001314077.2:c.697+32T>C	NP_001301006.1:n.697+32T>C