Canonical Allele Identifier: CA494925815
Gene: VKORC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.31102473G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091152G>A , CM000678.2:g.31091152G>A GRCh38
NC_000016.9:g.31102473G>A , CM000678.1:g.31102473G>A GRCh37
NC_000016.8:g.31009974G>A NCBI36
NG_011564.1:g.8804C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.474C>T MANE Select ENSP00000378426.2:p.Gly158=
ENST00000300851.10:c.*85C>T ENSP00000300851.6:n.*85C>T
ENST00000319788.11:c.*85C>T ENSP00000326135.7:n.*85C>T
ENST00000354895.4:c.*85C>T ENSP00000346969.4:n.*85C>T
ENST00000394971.7:c.*85C>T ENSP00000378422.3:n.*85C>T
ENST00000394975.2:c.474C>T ENSP00000378426.2:p.Gly158=
ENST00000420057.2:c.436C>T
ENST00000529564.1:c.283+2160C>T ENSP00000431371.1:n.283+2160C>T
ENST00000532364.1:c.173+3405C>T ENSP00000460316.1:n.173+3405C>T
ENST00000533518.5:c.347C>T
NM_001311311.1:c.558C>T NP_001298240.1:p.Gly186=
NM_024006.4:c.474C>T NP_076869.1:p.Gly158=
NM_024006.5:c.474C>T NP_076869.1:p.Gly158=
NM_206824.1:c.*85C>T NP_996560.1:n.*85C>T
NM_206824.2:c.*85C>T NP_996560.1:n.*85C>T
XM_011545944.1:c.474C>T XP_011544246.1:p.Gly158=
XM_011545945.1:c.*85C>T XP_011544247.1:n.*85C>T
XR_950848.1:n.1262C>T
NM_024006.6:c.474C>T MANE Select NP_076869.1:p.Gly158=
NM_001311311.2:c.558C>T NP_001298240.1:p.Gly186=
NM_206824.3:c.*85C>T NP_996560.1:n.*85C>T