Canonical Allele Identifier: CA280619941

Gene: VKORC1

Linked Data

• dbSNP Id: rs1022061765
• gnomAD v3: 16-31091249-A-G
• gnomAD v4: 16-31091249-A-G
• MyVariant Identifiers: chr16:g.31102570A>G (hg19) ; chr16:g.31091249A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091249A>G , CM000678.2:g.31091249A>G	GRCh38
NC_000016.9:g.31102570A>G , CM000678.1:g.31102570A>G	GRCh37
NC_000016.8:g.31010071A>G	NCBI36
NG_011564.1:g.8707T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.377T>C MANE Select	ENSP00000378426.2:p.Phe126Ser
ENST00000300851.10:c.438T>C	ENSP00000300851.6:p.Leu146=
ENST00000319788.11:c.459T>C	ENSP00000326135.7:p.Leu153=
ENST00000354895.4:c.267T>C	ENSP00000346969.4:p.Leu89=
ENST00000394971.7:c.471T>C	ENSP00000378422.3:p.Leu157=
ENST00000394975.2:c.377T>C	ENSP00000378426.2:p.Phe126Ser
ENST00000420057.2:c.339T>C
ENST00000472468.1:c.62T>C	ENSP00000458994.1:p.Phe21Ser
ENST00000498155.1:c.474T>C	ENSP00000417662.1:p.Leu158=
ENST00000529564.1:c.283+2063T>C	ENSP00000431371.1:n.283+2063T>C
ENST00000532364.1:c.173+3308T>C	ENSP00000460316.1:n.173+3308T>C
ENST00000533518.5:c.250T>C
NM_001311311.1:c.461T>C	NP_001298240.1:p.Phe154Ser
NM_024006.4:c.377T>C	NP_076869.1:p.Phe126Ser
NM_024006.5:c.377T>C	NP_076869.1:p.Phe126Ser
NM_206824.1:c.267T>C	NP_996560.1:p.Leu89=
NM_206824.2:c.267T>C	NP_996560.1:p.Leu89=
XM_011545944.1:c.377T>C	XP_011544246.1:p.Phe126Ser
XM_011545945.1:c.267T>C	XP_011544247.1:p.Leu89=
XR_950848.1:n.1165T>C
NM_024006.6:c.377T>C MANE Select	NP_076869.1:p.Phe126Ser
NM_001311311.2:c.461T>C	NP_001298240.1:p.Phe154Ser
NM_206824.3:c.267T>C	NP_996560.1:p.Leu89=