Canonical Allele Identifier: CA2703417138

Gene: PROS1

Linked Data

• dbSNP Id: rs2107158023

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898410G>C , CM000665.2:g.93898410G>C	GRCh38
NC_000003.11:g.93617254G>C , CM000665.1:g.93617254G>C	GRCh37
NC_000003.10:g.95099944G>C	NCBI36
NG_009813.1:g.80681C>G , LRG_572:g.80681C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.849+38C>G	ENSP00000330021.7:n.849+38C>G
ENST00000394236.9:c.849+38C>G MANE Select	ENSP00000377783.3:n.849+38C>G
ENST00000407433.6:c.804+38C>G	ENSP00000385794.2:n.804+38C>G
ENST00000647936.1:c.849+38C>G	ENSP00000496822.1:n.849+38C>G
ENST00000648381.1:n.1017+38C>G
ENST00000648853.1:c.807+38C>G	ENSP00000497262.1:n.807+38C>G
ENST00000649103.1:c.948+38C>G	ENSP00000497962.1:n.948+38C>G
ENST00000650591.1:c.945+38C>G	ENSP00000497376.1:n.945+38C>G
ENST00000394236.7:c.849+38C>G	ENSP00000377783.3:n.849+38C>G
ENST00000407433.5:c.456+38C>G	ENSP00000385794.1:n.456+38C>G
NM_000313.3:c.849+38C>G , LRG_572t1:c.849+38C>G	NP_000304.2:n.849+38C>G
NM_001314077.1:c.945+38C>G , LRG_572t2:c.945+38C>G	NP_001301006.1:n.945+38C>G
NM_000313.4:c.849+38C>G MANE Select	NP_000304.2:n.849+38C>G
NM_001314077.2:c.945+38C>G	NP_001301006.1:n.945+38C>G