Canonical Allele Identifier: CA395729711

Gene: VKORC1

Linked Data

• dbSNP Id: rs1361180864
• gnomAD v2: 16-31102577-G-C
• gnomAD v4: 16-31091256-G-C
• MyVariant Identifiers: chr16:g.31102577G>C (hg19) ; chr16:g.31091256G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091256G>C , CM000678.2:g.31091256G>C	GRCh38
NC_000016.9:g.31102577G>C , CM000678.1:g.31102577G>C	GRCh37
NC_000016.8:g.31010078G>C	NCBI36
NG_011564.1:g.8700C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.370C>G MANE Select	ENSP00000378426.2:p.Leu124Val
ENST00000300851.10:c.431C>G	ENSP00000300851.6:p.Pro144Arg
ENST00000319788.11:c.452C>G	ENSP00000326135.7:p.Pro151Arg
ENST00000354895.4:c.260C>G	ENSP00000346969.4:p.Pro87Arg
ENST00000394971.7:c.464C>G	ENSP00000378422.3:p.Pro155Arg
ENST00000394975.2:c.370C>G	ENSP00000378426.2:p.Leu124Val
ENST00000420057.2:c.332C>G
ENST00000472468.1:c.55C>G	ENSP00000458994.1:p.Leu19Val
ENST00000498155.1:c.467C>G	ENSP00000417662.1:p.Pro156Arg
ENST00000529564.1:c.283+2056C>G	ENSP00000431371.1:n.283+2056C>G
ENST00000532364.1:c.173+3301C>G	ENSP00000460316.1:n.173+3301C>G
ENST00000533518.5:c.243C>G
NM_001311311.1:c.454C>G	NP_001298240.1:p.Leu152Val
NM_024006.4:c.370C>G	NP_076869.1:p.Leu124Val
NM_024006.5:c.370C>G	NP_076869.1:p.Leu124Val
NM_206824.1:c.260C>G	NP_996560.1:p.Pro87Arg
NM_206824.2:c.260C>G	NP_996560.1:p.Pro87Arg
XM_011545944.1:c.370C>G	XP_011544246.1:p.Leu124Val
XM_011545945.1:c.260C>G	XP_011544247.1:p.Pro87Arg
XR_950848.1:n.1158C>G
NM_024006.6:c.370C>G MANE Select	NP_076869.1:p.Leu124Val
NM_001311311.2:c.454C>G	NP_001298240.1:p.Leu152Val
NM_206824.3:c.260C>G	NP_996560.1:p.Pro87Arg