Canonical Allele Identifier: CA78520146

Gene: PROS1

Linked Data

• dbSNP Id: rs147324335
• MyVariant Identifiers: chr3:g.93593130G>T (hg19) ; chr3:g.93874286G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874286G>T , CM000665.2:g.93874286G>T	GRCh38
NC_000003.11:g.93593130G>T , CM000665.1:g.93593130G>T	GRCh37
NC_000003.10:g.95075820G>T	NCBI36
NG_009813.1:g.104805C>A , LRG_572:g.104805C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1990C>A	ENSP00000330021.7:p.His664Asn
ENST00000394236.9:c.1990C>A MANE Select	ENSP00000377783.3:p.His664Asn
ENST00000407433.6:c.1945C>A	ENSP00000385794.2:p.His649Asn
ENST00000647936.1:c.*93C>A	ENSP00000496822.1:n.*93C>A
ENST00000648381.1:n.2158C>A
ENST00000648853.1:c.1948C>A	ENSP00000497262.1:p.His650Asn
ENST00000650591.1:c.2086C>A	ENSP00000497376.1:p.His696Asn
ENST00000394236.7:c.1990C>A	ENSP00000377783.3:p.His664Asn
ENST00000407433.5:c.1597C>A	ENSP00000385794.1:p.His533Asn
NM_000313.3:c.1990C>A , LRG_572t1:c.1990C>A	NP_000304.2:p.His664Asn
NM_001314077.1:c.2086C>A , LRG_572t2:c.2086C>A	NP_001301006.1:p.His696Asn
NM_000313.4:c.1990C>A MANE Select	NP_000304.2:p.His664Asn
NM_001314077.2:c.2086C>A	NP_001301006.1:p.His696Asn