Canonical Allele Identifier: CA395732589

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31105903T>G (hg19) ; chr16:g.31094582T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094582T>G , CM000678.2:g.31094582T>G	GRCh38
NC_000016.9:g.31105903T>G , CM000678.1:g.31105903T>G	GRCh37
NC_000016.8:g.31013404T>G	NCBI36
NG_011564.1:g.5374A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.148A>C MANE Select	ENSP00000378426.2:p.Ser50Arg
ENST00000300851.10:c.148A>C	ENSP00000300851.6:p.Ser50Arg
ENST00000319788.11:c.148A>C	ENSP00000326135.7:p.Ser50Arg
ENST00000354895.4:c.148A>C	ENSP00000346969.4:p.Ser50Arg
ENST00000394975.2:c.148A>C	ENSP00000378426.2:p.Ser50Arg
ENST00000420057.2:c.245+807A>C
ENST00000498155.1:c.270+807A>C	ENSP00000417662.1:n.270+807A>C
ENST00000529564.1:c.148A>C	ENSP00000431371.1:p.Ser50Arg
ENST00000532364.1:c.148A>C	ENSP00000460316.1:p.Ser50Arg
ENST00000533518.5:c.21A>C
NM_001311311.1:c.148A>C	NP_001298240.1:p.Ser50Arg
NM_024006.4:c.148A>C	NP_076869.1:p.Ser50Arg
NM_024006.5:c.148A>C	NP_076869.1:p.Ser50Arg
NM_206824.1:c.148A>C	NP_996560.1:p.Ser50Arg
NM_206824.2:c.148A>C	NP_996560.1:p.Ser50Arg
XM_011545944.1:c.148A>C	XP_011544246.1:p.Ser50Arg
XM_011545945.1:c.148A>C	XP_011544247.1:p.Ser50Arg
XR_950848.1:n.936A>C
NM_024006.6:c.148A>C MANE Select	NP_076869.1:p.Ser50Arg
NM_001311311.2:c.148A>C	NP_001298240.1:p.Ser50Arg
NM_206824.3:c.148A>C	NP_996560.1:p.Ser50Arg