Canonical Allele Identifier: CA2632821182

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31090864-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090864A>C , CM000678.2:g.31090864A>C	GRCh38
NC_000016.9:g.31102185A>C , CM000678.1:g.31102185A>C	GRCh37
NC_000016.8:g.31009686A>C	NCBI36
NG_011564.1:g.9092T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*270T>G MANE Select	ENSP00000378426.2:n.*270T>G
ENST00000300851.10:c.*373T>G	ENSP00000300851.6:n.*373T>G
ENST00000319788.11:c.*373T>G	ENSP00000326135.7:n.*373T>G
ENST00000354895.4:c.*373T>G	ENSP00000346969.4:n.*373T>G
ENST00000394975.2:c.*270T>G	ENSP00000378426.2:n.*270T>G
ENST00000420057.2:c.724T>G
ENST00000529564.1:c.283+2448T>G	ENSP00000431371.1:n.283+2448T>G
ENST00000532364.1:c.173+3693T>G	ENSP00000460316.1:n.173+3693T>G
ENST00000533518.5:c.407+228T>G
NM_001311311.1:c.*270T>G	NP_001298240.1:n.*270T>G
NM_024006.4:c.*270T>G	NP_076869.1:n.*270T>G
NM_024006.5:c.*270T>G	NP_076869.1:n.*270T>G
NM_206824.1:c.*373T>G	NP_996560.1:n.*373T>G
NM_206824.2:c.*373T>G	NP_996560.1:n.*373T>G
XM_011545944.1:c.*270T>G	XP_011544246.1:n.*270T>G
XM_011545945.1:c.*373T>G	XP_011544247.1:n.*373T>G
XR_950848.1:n.1550T>G
NM_024006.6:c.*270T>G MANE Select	NP_076869.1:n.*270T>G
NM_001311311.2:c.*270T>G	NP_001298240.1:n.*270T>G
NM_206824.3:c.*373T>G	NP_996560.1:n.*373T>G