Canonical Allele Identifier: CA8021134

Gene: VKORC1

Linked Data

• dbSNP Id: rs72547528
• ExAC: 16:31102655 G / C
• gnomAD v2: 16-31102655-G-C
• gnomAD v4: 16-31091334-G-C
• MyVariant Identifiers: chr16:g.31102655G>C (hg19) ; chr16:g.31091334G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091334G>C , CM000678.2:g.31091334G>C	GRCh38
NC_000016.9:g.31102655G>C , CM000678.1:g.31102655G>C	GRCh37
NC_000016.8:g.31010156G>C	NCBI36
NG_011564.1:g.8622C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.292C>G MANE Select	ENSP00000378426.2:p.Arg98Gly
ENST00000300851.10:c.353C>G	ENSP00000300851.6:p.Ala118Gly
ENST00000319788.11:c.374C>G	ENSP00000326135.7:p.Ala125Gly
ENST00000354895.4:c.182C>G	ENSP00000346969.4:p.Ala61Gly
ENST00000394971.7:c.386C>G	ENSP00000378422.3:p.Ala129Gly
ENST00000394975.2:c.292C>G	ENSP00000378426.2:p.Arg98Gly
ENST00000420057.2:c.254C>G
ENST00000472468.1:c.-24C>G	ENSP00000458994.1:n.-24C>G
ENST00000498155.1:c.389C>G	ENSP00000417662.1:p.Ala130Gly
ENST00000529564.1:c.283+1978C>G	ENSP00000431371.1:n.283+1978C>G
ENST00000532364.1:c.173+3223C>G	ENSP00000460316.1:n.173+3223C>G
ENST00000533518.5:c.165C>G
NM_001311311.1:c.376C>G	NP_001298240.1:p.Arg126Gly
NM_024006.4:c.292C>G	NP_076869.1:p.Arg98Gly
NM_024006.5:c.292C>G	NP_076869.1:p.Arg98Gly
NM_206824.1:c.182C>G	NP_996560.1:p.Ala61Gly
NM_206824.2:c.182C>G	NP_996560.1:p.Ala61Gly
XM_011545944.1:c.292C>G	XP_011544246.1:p.Arg98Gly
XM_011545945.1:c.182C>G	XP_011544247.1:p.Ala61Gly
XR_950848.1:n.1080C>G
NM_024006.6:c.292C>G MANE Select	NP_076869.1:p.Arg98Gly
NM_001311311.2:c.376C>G	NP_001298240.1:p.Arg126Gly
NM_206824.3:c.182C>G	NP_996560.1:p.Ala61Gly