Canonical Allele Identifier: CA494708009

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31105901G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094580G>A , CM000678.2:g.31094580G>A	GRCh38
NC_000016.9:g.31105901G>A , CM000678.1:g.31105901G>A	GRCh37
NC_000016.8:g.31013402G>A	NCBI36
NG_011564.1:g.5376C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.150C>T MANE Select	ENSP00000378426.2:p.Ser50=
ENST00000300851.10:c.150C>T	ENSP00000300851.6:p.Ser50=
ENST00000319788.11:c.150C>T	ENSP00000326135.7:p.Ser50=
ENST00000354895.4:c.150C>T	ENSP00000346969.4:p.Ser50=
ENST00000394975.2:c.150C>T	ENSP00000378426.2:p.Ser50=
ENST00000420057.2:c.245+809C>T
ENST00000498155.1:c.270+809C>T	ENSP00000417662.1:n.270+809C>T
ENST00000529564.1:c.150C>T	ENSP00000431371.1:p.Ser50=
ENST00000532364.1:c.150C>T	ENSP00000460316.1:p.Ser50=
ENST00000533518.5:c.23C>T
NM_001311311.1:c.150C>T	NP_001298240.1:p.Ser50=
NM_024006.4:c.150C>T	NP_076869.1:p.Ser50=
NM_024006.5:c.150C>T	NP_076869.1:p.Ser50=
NM_206824.1:c.150C>T	NP_996560.1:p.Ser50=
NM_206824.2:c.150C>T	NP_996560.1:p.Ser50=
XM_011545944.1:c.150C>T	XP_011544246.1:p.Ser50=
XM_011545945.1:c.150C>T	XP_011544247.1:p.Ser50=
XR_950848.1:n.938C>T
NM_024006.6:c.150C>T MANE Select	NP_076869.1:p.Ser50=
NM_001311311.2:c.150C>T	NP_001298240.1:p.Ser50=
NM_206824.3:c.150C>T	NP_996560.1:p.Ser50=