Canonical Allele Identifier: CA8021132

Gene: VKORC1

Linked Data

• dbSNP Id: rs760391247
• ExAC: 16:31102603 G / C
• gnomAD v2: 16-31102603-G-C
• gnomAD v4: 16-31091282-G-C
• MyVariant Identifiers: chr16:g.31102603G>C (hg19) ; chr16:g.31091282G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091282G>C , CM000678.2:g.31091282G>C	GRCh38
NC_000016.9:g.31102603G>C , CM000678.1:g.31102603G>C	GRCh37
NC_000016.8:g.31010104G>C	NCBI36
NG_011564.1:g.8674C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.344C>G MANE Select	ENSP00000378426.2:p.Ala115Gly
ENST00000300851.10:c.405C>G	ENSP00000300851.6:p.Arg135=
ENST00000319788.11:c.426C>G	ENSP00000326135.7:p.Arg142=
ENST00000354895.4:c.234C>G	ENSP00000346969.4:p.Arg78=
ENST00000394971.7:c.438C>G	ENSP00000378422.3:p.Arg146=
ENST00000394975.2:c.344C>G	ENSP00000378426.2:p.Ala115Gly
ENST00000420057.2:c.306C>G
ENST00000472468.1:c.29C>G	ENSP00000458994.1:p.Ala10Gly
ENST00000498155.1:c.441C>G	ENSP00000417662.1:p.Arg147=
ENST00000529564.1:c.283+2030C>G	ENSP00000431371.1:n.283+2030C>G
ENST00000532364.1:c.173+3275C>G	ENSP00000460316.1:n.173+3275C>G
ENST00000533518.5:c.217C>G
NM_001311311.1:c.428C>G	NP_001298240.1:p.Ala143Gly
NM_024006.4:c.344C>G	NP_076869.1:p.Ala115Gly
NM_024006.5:c.344C>G	NP_076869.1:p.Ala115Gly
NM_206824.1:c.234C>G	NP_996560.1:p.Arg78=
NM_206824.2:c.234C>G	NP_996560.1:p.Arg78=
XM_011545944.1:c.344C>G	XP_011544246.1:p.Ala115Gly
XM_011545945.1:c.234C>G	XP_011544247.1:p.Arg78=
XR_950848.1:n.1132C>G
NM_024006.6:c.344C>G MANE Select	NP_076869.1:p.Ala115Gly
NM_001311311.2:c.428C>G	NP_001298240.1:p.Ala143Gly
NM_206824.3:c.234C>G	NP_996560.1:p.Arg78=