Canonical Allele Identifier: CA8021108

Gene: VKORC1

Linked Data

• dbSNP Id: rs749165172
• ExAC: 16:31102426 A / T
• gnomAD v2: 16-31102426-A-T
• gnomAD v3: 16-31091105-A-T
• gnomAD v4: 16-31091105-A-T
• MyVariant Identifiers: chr16:g.31102426A>T (hg19) ; chr16:g.31091105A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091105A>T , CM000678.2:g.31091105A>T	GRCh38
NC_000016.9:g.31102426A>T , CM000678.1:g.31102426A>T	GRCh37
NC_000016.8:g.31009927A>T	NCBI36
NG_011564.1:g.8851T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*29T>A MANE Select	ENSP00000378426.2:n.*29T>A
ENST00000300851.10:c.*132T>A	ENSP00000300851.6:n.*132T>A
ENST00000319788.11:c.*132T>A	ENSP00000326135.7:n.*132T>A
ENST00000354895.4:c.*132T>A	ENSP00000346969.4:n.*132T>A
ENST00000394971.7:c.*132T>A	ENSP00000378422.3:n.*132T>A
ENST00000394975.2:c.*29T>A	ENSP00000378426.2:n.*29T>A
ENST00000420057.2:c.483T>A
ENST00000529564.1:c.283+2207T>A	ENSP00000431371.1:n.283+2207T>A
ENST00000532364.1:c.173+3452T>A	ENSP00000460316.1:n.173+3452T>A
ENST00000533518.5:c.394T>A
NM_001311311.1:c.*29T>A	NP_001298240.1:n.*29T>A
NM_024006.4:c.*29T>A	NP_076869.1:n.*29T>A
NM_024006.5:c.*29T>A	NP_076869.1:n.*29T>A
NM_206824.1:c.*132T>A	NP_996560.1:n.*132T>A
NM_206824.2:c.*132T>A	NP_996560.1:n.*132T>A
XM_011545944.1:c.*29T>A	XP_011544246.1:n.*29T>A
XM_011545945.1:c.*132T>A	XP_011544247.1:n.*132T>A
XR_950848.1:n.1309T>A
NM_024006.6:c.*29T>A MANE Select	NP_076869.1:n.*29T>A
NM_001311311.2:c.*29T>A	NP_001298240.1:n.*29T>A
NM_206824.3:c.*132T>A	NP_996560.1:n.*132T>A