Canonical Allele Identifier: CA115412
Gene: VKORC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2207
ClinVar RCV Id: RCV000002291
dbSNP Id: rs104894539

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31094645C>A , CM000678.2:g.31094645C>A GRCh38
NC_000016.9:g.31105966C>A , CM000678.1:g.31105966C>A GRCh37
NC_000016.8:g.31013467C>A NCBI36
NG_011564.1:g.5311G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.85G>T MANE Select ENSP00000378426.2:p.Val29Leu
ENST00000300851.10:c.85G>T ENSP00000300851.6:p.Val29Leu
ENST00000319788.11:c.85G>T ENSP00000326135.7:p.Val29Leu
ENST00000354895.4:c.85G>T ENSP00000346969.4:p.Val29Leu
ENST00000394975.2:c.85G>T ENSP00000378426.2:p.Val29Leu
ENST00000420057.2:c.245+744G>T
ENST00000498155.1:c.270+744G>T ENSP00000417662.1:n.270+744G>T
ENST00000529564.1:c.85G>T ENSP00000431371.1:p.Val29Leu
ENST00000532364.1:c.85G>T ENSP00000460316.1:p.Val29Leu
NM_001311311.1:c.85G>T NP_001298240.1:p.Val29Leu
NM_024006.4:c.85G>T NP_076869.1:p.Val29Leu
NM_024006.5:c.85G>T NP_076869.1:p.Val29Leu
NM_206824.1:c.85G>T NP_996560.1:p.Val29Leu
NM_206824.2:c.85G>T NP_996560.1:p.Val29Leu
XM_011545944.1:c.85G>T XP_011544246.1:p.Val29Leu
XM_011545945.1:c.85G>T XP_011544247.1:p.Val29Leu
XR_950848.1:n.873G>T
NM_024006.6:c.85G>T MANE Select NP_076869.1:p.Val29Leu
NM_001311311.2:c.85G>T NP_001298240.1:p.Val29Leu
NM_206824.3:c.85G>T NP_996560.1:p.Val29Leu