Canonical Allele Identifier: CA494708186

Gene: VKORC1

Linked Data

• dbSNP Id: rs1209100404
• gnomAD v2: 16-31105928-C-A
• gnomAD v4: 16-31094607-C-A
• MyVariant Identifiers: chr16:g.31105928C>A (hg19) ; chr16:g.31094607C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094607C>A , CM000678.2:g.31094607C>A	GRCh38
NC_000016.9:g.31105928C>A , CM000678.1:g.31105928C>A	GRCh37
NC_000016.8:g.31013429C>A	NCBI36
NG_011564.1:g.5349G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.123G>T MANE Select	ENSP00000378426.2:p.Ala41=
ENST00000300851.10:c.123G>T	ENSP00000300851.6:p.Ala41=
ENST00000319788.11:c.123G>T	ENSP00000326135.7:p.Ala41=
ENST00000354895.4:c.123G>T	ENSP00000346969.4:p.Ala41=
ENST00000394975.2:c.123G>T	ENSP00000378426.2:p.Ala41=
ENST00000420057.2:c.245+782G>T
ENST00000498155.1:c.270+782G>T	ENSP00000417662.1:n.270+782G>T
ENST00000529564.1:c.123G>T	ENSP00000431371.1:p.Ala41=
ENST00000532364.1:c.123G>T	ENSP00000460316.1:p.Ala41=
NM_001311311.1:c.123G>T	NP_001298240.1:p.Ala41=
NM_024006.4:c.123G>T	NP_076869.1:p.Ala41=
NM_024006.5:c.123G>T	NP_076869.1:p.Ala41=
NM_206824.1:c.123G>T	NP_996560.1:p.Ala41=
NM_206824.2:c.123G>T	NP_996560.1:p.Ala41=
XM_011545944.1:c.123G>T	XP_011544246.1:p.Ala41=
XM_011545945.1:c.123G>T	XP_011544247.1:p.Ala41=
XR_950848.1:n.911G>T
NM_024006.6:c.123G>T MANE Select	NP_076869.1:p.Ala41=
NM_001311311.2:c.123G>T	NP_001298240.1:p.Ala41=
NM_206824.3:c.123G>T	NP_996560.1:p.Ala41=