Canonical Allele Identifier: CA494925951
Gene: VKORC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.31102563G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091242G>A , CM000678.2:g.31091242G>A GRCh38
NC_000016.9:g.31102563G>A , CM000678.1:g.31102563G>A GRCh37
NC_000016.8:g.31010064G>A NCBI36
NG_011564.1:g.8714C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.384C>T MANE Select ENSP00000378426.2:p.Leu128=
ENST00000300851.10:c.445C>T ENSP00000300851.6:p.Leu149=
ENST00000319788.11:c.466C>T ENSP00000326135.7:p.Leu156=
ENST00000354895.4:c.274C>T ENSP00000346969.4:p.Leu92=
ENST00000394971.7:c.478C>T ENSP00000378422.3:p.Leu160=
ENST00000394975.2:c.384C>T ENSP00000378426.2:p.Leu128=
ENST00000420057.2:c.346C>T
ENST00000472468.1:c.69C>T ENSP00000458994.1:p.Leu23=
ENST00000498155.1:c.481C>T ENSP00000417662.1:p.Leu161=
ENST00000529564.1:c.283+2070C>T ENSP00000431371.1:n.283+2070C>T
ENST00000532364.1:c.173+3315C>T ENSP00000460316.1:n.173+3315C>T
ENST00000533518.5:c.257C>T
NM_001311311.1:c.468C>T NP_001298240.1:p.Leu156=
NM_024006.4:c.384C>T NP_076869.1:p.Leu128=
NM_024006.5:c.384C>T NP_076869.1:p.Leu128=
NM_206824.1:c.274C>T NP_996560.1:p.Leu92=
NM_206824.2:c.274C>T NP_996560.1:p.Leu92=
XM_011545944.1:c.384C>T XP_011544246.1:p.Leu128=
XM_011545945.1:c.274C>T XP_011544247.1:p.Leu92=
XR_950848.1:n.1172C>T
NM_024006.6:c.384C>T MANE Select NP_076869.1:p.Leu128=
NM_001311311.2:c.468C>T NP_001298240.1:p.Leu156=
NM_206824.3:c.274C>T NP_996560.1:p.Leu92=