Canonical Allele Identifier: CA622171486

Gene: VKORC1

Linked Data

• dbSNP Id: rs1203390842
• gnomAD v2: 16-31102441-C-T
• gnomAD v4: 16-31091120-C-T
• MyVariant Identifiers: chr16:g.31102441C>T (hg19) ; chr16:g.31091120C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091120C>T , CM000678.2:g.31091120C>T	GRCh38
NC_000016.9:g.31102441C>T , CM000678.1:g.31102441C>T	GRCh37
NC_000016.8:g.31009942C>T	NCBI36
NG_011564.1:g.8836G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*14G>A MANE Select	ENSP00000378426.2:n.*14G>A
ENST00000300851.10:c.*117G>A	ENSP00000300851.6:n.*117G>A
ENST00000319788.11:c.*117G>A	ENSP00000326135.7:n.*117G>A
ENST00000354895.4:c.*117G>A	ENSP00000346969.4:n.*117G>A
ENST00000394971.7:c.*117G>A	ENSP00000378422.3:n.*117G>A
ENST00000394975.2:c.*14G>A	ENSP00000378426.2:n.*14G>A
ENST00000420057.2:c.468G>A
ENST00000529564.1:c.283+2192G>A	ENSP00000431371.1:n.283+2192G>A
ENST00000532364.1:c.173+3437G>A	ENSP00000460316.1:n.173+3437G>A
ENST00000533518.5:c.379G>A
NM_001311311.1:c.*14G>A	NP_001298240.1:n.*14G>A
NM_024006.4:c.*14G>A	NP_076869.1:n.*14G>A
NM_024006.5:c.*14G>A	NP_076869.1:n.*14G>A
NM_206824.1:c.*117G>A	NP_996560.1:n.*117G>A
NM_206824.2:c.*117G>A	NP_996560.1:n.*117G>A
XM_011545944.1:c.*14G>A	XP_011544246.1:n.*14G>A
XM_011545945.1:c.*117G>A	XP_011544247.1:n.*117G>A
XR_950848.1:n.1294G>A
NM_024006.6:c.*14G>A MANE Select	NP_076869.1:n.*14G>A
NM_001311311.2:c.*14G>A	NP_001298240.1:n.*14G>A
NM_206824.3:c.*117G>A	NP_996560.1:n.*117G>A