Canonical Allele Identifier: CA912682979

Gene: PROS1

Linked Data

• dbSNP Id: rs1413446803
• MyVariant Identifiers: chr3:g.93592588T>C (hg19) ; chr3:g.93873744T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873744T>C , CM000665.2:g.93873744T>C	GRCh38
NC_000003.11:g.93592588T>C , CM000665.1:g.93592588T>C	GRCh37
NC_000003.10:g.95075278T>C	NCBI36
NG_009813.1:g.105347A>G , LRG_572:g.105347A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*2-331A>G	ENSP00000330021.7:n.*2-331A>G
ENST00000394236.9:c.*501A>G MANE Select	ENSP00000377783.3:n.*501A>G
ENST00000407433.6:c.*501A>G	ENSP00000385794.2:n.*501A>G
ENST00000647936.1:c.*635A>G	ENSP00000496822.1:n.*635A>G
ENST00000648381.1:n.2700A>G
ENST00000648853.1:c.*501A>G	ENSP00000497262.1:n.*501A>G
ENST00000650591.1:c.*501A>G	ENSP00000497376.1:n.*501A>G
ENST00000394236.7:c.*501A>G	ENSP00000377783.3:n.*501A>G
ENST00000407433.5:c.*501A>G	ENSP00000385794.1:n.*501A>G
NM_000313.3:c.*501A>G , LRG_572t1:c.*501A>G	NP_000304.2:n.*501A>G
NM_001314077.1:c.*501A>G , LRG_572t2:c.*501A>G	NP_001301006.1:n.*501A>G
NM_000313.4:c.*501A>G MANE Select	NP_000304.2:n.*501A>G
NM_001314077.2:c.*501A>G	NP_001301006.1:n.*501A>G