Canonical Allele Identifier: CA395732699

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31094612-G-T
• MyVariant Identifiers: chr16:g.31105933G>T (hg19) ; chr16:g.31094612G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094612G>T , CM000678.2:g.31094612G>T	GRCh38
NC_000016.9:g.31105933G>T , CM000678.1:g.31105933G>T	GRCh37
NC_000016.8:g.31013434G>T	NCBI36
NG_011564.1:g.5344C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.118C>A MANE Select	ENSP00000378426.2:p.Arg40Ser
ENST00000300851.10:c.118C>A	ENSP00000300851.6:p.Arg40Ser
ENST00000319788.11:c.118C>A	ENSP00000326135.7:p.Arg40Ser
ENST00000354895.4:c.118C>A	ENSP00000346969.4:p.Arg40Ser
ENST00000394975.2:c.118C>A	ENSP00000378426.2:p.Arg40Ser
ENST00000420057.2:c.245+777C>A
ENST00000498155.1:c.270+777C>A	ENSP00000417662.1:n.270+777C>A
ENST00000529564.1:c.118C>A	ENSP00000431371.1:p.Arg40Ser
ENST00000532364.1:c.118C>A	ENSP00000460316.1:p.Arg40Ser
NM_001311311.1:c.118C>A	NP_001298240.1:p.Arg40Ser
NM_024006.4:c.118C>A	NP_076869.1:p.Arg40Ser
NM_024006.5:c.118C>A	NP_076869.1:p.Arg40Ser
NM_206824.1:c.118C>A	NP_996560.1:p.Arg40Ser
NM_206824.2:c.118C>A	NP_996560.1:p.Arg40Ser
XM_011545944.1:c.118C>A	XP_011544246.1:p.Arg40Ser
XM_011545945.1:c.118C>A	XP_011544247.1:p.Arg40Ser
XR_950848.1:n.906C>A
NM_024006.6:c.118C>A MANE Select	NP_076869.1:p.Arg40Ser
NM_001311311.2:c.118C>A	NP_001298240.1:p.Arg40Ser
NM_206824.3:c.118C>A	NP_996560.1:p.Arg40Ser