Canonical Allele Identifier: CA395729995

Gene: VKORC1

Linked Data

• dbSNP Id: rs1389762752
• gnomAD v2: 16-31102636-A-C
• gnomAD v4: 16-31091315-A-C
• MyVariant Identifiers: chr16:g.31102636A>C (hg19) ; chr16:g.31091315A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091315A>C , CM000678.2:g.31091315A>C	GRCh38
NC_000016.9:g.31102636A>C , CM000678.1:g.31102636A>C	GRCh37
NC_000016.8:g.31010137A>C	NCBI36
NG_011564.1:g.8641T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.311T>G MANE Select	ENSP00000378426.2:p.Val104Gly
ENST00000300851.10:c.372T>G	ENSP00000300851.6:p.Cys124Trp
ENST00000319788.11:c.393T>G	ENSP00000326135.7:p.Cys131Trp
ENST00000354895.4:c.201T>G	ENSP00000346969.4:p.Cys67Trp
ENST00000394971.7:c.405T>G	ENSP00000378422.3:p.Cys135Trp
ENST00000394975.2:c.311T>G	ENSP00000378426.2:p.Val104Gly
ENST00000420057.2:c.273T>G
ENST00000472468.1:c.-5T>G	ENSP00000458994.1:n.-5T>G
ENST00000498155.1:c.408T>G	ENSP00000417662.1:p.Cys136Trp
ENST00000529564.1:c.283+1997T>G	ENSP00000431371.1:n.283+1997T>G
ENST00000532364.1:c.173+3242T>G	ENSP00000460316.1:n.173+3242T>G
ENST00000533518.5:c.184T>G
NM_001311311.1:c.395T>G	NP_001298240.1:p.Val132Gly
NM_024006.4:c.311T>G	NP_076869.1:p.Val104Gly
NM_024006.5:c.311T>G	NP_076869.1:p.Val104Gly
NM_206824.1:c.201T>G	NP_996560.1:p.Cys67Trp
NM_206824.2:c.201T>G	NP_996560.1:p.Cys67Trp
XM_011545944.1:c.311T>G	XP_011544246.1:p.Val104Gly
XM_011545945.1:c.201T>G	XP_011544247.1:p.Cys67Trp
XR_950848.1:n.1099T>G
NM_024006.6:c.311T>G MANE Select	NP_076869.1:p.Val104Gly
NM_001311311.2:c.395T>G	NP_001298240.1:p.Val132Gly
NM_206824.3:c.201T>G	NP_996560.1:p.Cys67Trp