Canonical Allele Identifier: CA10643478

Gene: VKORC1

Linked Data

• ClinVar Variation Id: 318978
• ClinVar RCV Id: RCV000398380
• dbSNP Id: rs569737355
• gnomAD v2: 16-31106210-C-G
• gnomAD v3: 16-31094889-C-G
• gnomAD v4: 16-31094889-C-G
• MyVariant Identifiers: chr16:g.31106210C>G (hg19) ; chr16:g.31094889C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094889C>G , CM000678.2:g.31094889C>G	GRCh38
NC_000016.9:g.31106210C>G , CM000678.1:g.31106210C>G	GRCh37
NC_000016.8:g.31013711C>G	NCBI36
NG_011564.1:g.5067G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319788.11:c.-160G>C	ENSP00000326135.7:n.-160G>C
ENST00000354895.4:c.-160G>C	ENSP00000346969.4:n.-160G>C
ENST00000394975.2:c.-160G>C	ENSP00000378426.2:n.-160G>C
ENST00000420057.2:c.245+500G>C
ENST00000498155.1:c.270+500G>C	ENSP00000417662.1:n.270+500G>C
ENST00000529564.1:c.-160G>C	ENSP00000431371.1:n.-160G>C
ENST00000532364.1:c.-160G>C	ENSP00000460316.1:n.-160G>C
NM_001311311.1:c.-160G>C	NP_001298240.1:n.-160G>C
NM_024006.4:c.-160G>C	NP_076869.1:n.-160G>C
NM_024006.5:c.-160G>C	NP_076869.1:n.-160G>C
NM_206824.1:c.-160G>C	NP_996560.1:n.-160G>C
NM_206824.2:c.-160G>C	NP_996560.1:n.-160G>C
XM_011545944.1:c.-160G>C	XP_011544246.1:n.-160G>C
XM_011545945.1:c.-160G>C	XP_011544247.1:n.-160G>C
XR_950848.1:n.629G>C