Canonical Allele Identifier: CA494925816

Gene: VKORC1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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