Canonical Allele Identifier: CA353673001

Gene: PROS1

Linked Data

• dbSNP Id: rs1396796176
• gnomAD v2: 3-93617392-T-C
• gnomAD v4: 3-93898548-T-C
• MyVariant Identifiers: chr3:g.93617392T>C (hg19) ; chr3:g.93898548T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898548T>C , CM000665.2:g.93898548T>C	GRCh38
NC_000003.11:g.93617392T>C , CM000665.1:g.93617392T>C	GRCh37
NC_000003.10:g.95100082T>C	NCBI36
NG_009813.1:g.80543A>G , LRG_572:g.80543A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.749A>G	ENSP00000330021.7:p.Asn250Ser
ENST00000394236.9:c.749A>G MANE Select	ENSP00000377783.3:p.Asn250Ser
ENST00000407433.6:c.704A>G	ENSP00000385794.2:p.Asn235Ser
ENST00000647936.1:c.749A>G	ENSP00000496822.1:p.Asn250Ser
ENST00000648381.1:n.917A>G
ENST00000648853.1:c.707A>G	ENSP00000497262.1:p.Asn236Ser
ENST00000649103.1:c.848A>G	ENSP00000497962.1:n.848A>G
ENST00000650591.1:c.845A>G	ENSP00000497376.1:p.Asn282Ser
ENST00000394236.7:c.749A>G	ENSP00000377783.3:p.Asn250Ser
ENST00000407433.5:c.356A>G	ENSP00000385794.1:p.Asn119Ser
NM_000313.3:c.749A>G , LRG_572t1:c.749A>G	NP_000304.2:p.Asn250Ser
NM_001314077.1:c.845A>G , LRG_572t2:c.845A>G	NP_001301006.1:p.Asn282Ser
NM_000313.4:c.749A>G MANE Select	NP_000304.2:p.Asn250Ser
NM_001314077.2:c.845A>G	NP_001301006.1:p.Asn282Ser