Canonical Allele Identifier: CA115414
Gene: VKORC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2209
ClinVar RCV Id: RCV000002293
dbSNP Id: rs104894541

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31094558T>C , CM000678.2:g.31094558T>C GRCh38
NC_000016.9:g.31105879T>C , CM000678.1:g.31105879T>C GRCh37
NC_000016.8:g.31013380T>C NCBI36
NG_011564.1:g.5398A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.172A>G MANE Select ENSP00000378426.2:p.Arg58Gly
ENST00000300851.10:c.172A>G ENSP00000300851.6:p.Arg58Gly
ENST00000319788.11:c.172A>G ENSP00000326135.7:p.Arg58Gly
ENST00000354895.4:c.172A>G ENSP00000346969.4:p.Arg58Gly
ENST00000394975.2:c.172A>G ENSP00000378426.2:p.Arg58Gly
ENST00000420057.2:n.245+831A>G
ENST00000498155.1:c.270+831A>G ENSP00000417662.1:p.=
ENST00000529564.1:c.172A>G ENSP00000431371.1:p.Arg58Gly
ENST00000532364.1:c.172A>G ENSP00000460316.1:p.Arg58Gly
ENST00000533518.5:n.45A>G
NM_001311311.1:c.172A>G NP_001298240.1:p.Arg58Gly
NM_024006.4:c.172A>G NP_076869.1:p.Arg58Gly
NM_024006.5:c.172A>G NP_076869.1:p.Arg58Gly
NM_206824.1:c.172A>G NP_996560.1:p.Arg58Gly
NM_206824.2:c.172A>G NP_996560.1:p.Arg58Gly
XM_011545944.1:c.172A>G XP_011544246.1:p.Arg58Gly
XM_011545945.1:c.172A>G XP_011544247.1:p.Arg58Gly
XR_950848.1:n.960A>G
NM_024006.6:c.172A>G MANE Select NP_076869.1:p.Arg58Gly
NM_001311311.2:c.172A>G NP_001298240.1:p.Arg58Gly
NM_206824.3:c.172A>G NP_996560.1:p.Arg58Gly