Canonical Allele Identifier: CA2632821402

Gene: VKORC1

Linked Data

• gnomAD v4: 16-31091018-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091018G>C , CM000678.2:g.31091018G>C	GRCh38
NC_000016.9:g.31102339G>C , CM000678.1:g.31102339G>C	GRCh37
NC_000016.8:g.31009840G>C	NCBI36
NG_011564.1:g.8938C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.*116C>G MANE Select	ENSP00000378426.2:n.*116C>G
ENST00000300851.10:c.*219C>G	ENSP00000300851.6:n.*219C>G
ENST00000319788.11:c.*219C>G	ENSP00000326135.7:n.*219C>G
ENST00000354895.4:c.*219C>G	ENSP00000346969.4:n.*219C>G
ENST00000394975.2:c.*116C>G	ENSP00000378426.2:n.*116C>G
ENST00000420057.2:c.570C>G
ENST00000529564.1:c.283+2294C>G	ENSP00000431371.1:n.283+2294C>G
ENST00000532364.1:c.173+3539C>G	ENSP00000460316.1:n.173+3539C>G
ENST00000533518.5:c.407+74C>G
NM_001311311.1:c.*116C>G	NP_001298240.1:n.*116C>G
NM_024006.4:c.*116C>G	NP_076869.1:n.*116C>G
NM_024006.5:c.*116C>G	NP_076869.1:n.*116C>G
NM_206824.1:c.*219C>G	NP_996560.1:n.*219C>G
NM_206824.2:c.*219C>G	NP_996560.1:n.*219C>G
XM_011545944.1:c.*116C>G	XP_011544246.1:n.*116C>G
XM_011545945.1:c.*219C>G	XP_011544247.1:n.*219C>G
XR_950848.1:n.1396C>G
NM_024006.6:c.*116C>G MANE Select	NP_076869.1:n.*116C>G
NM_001311311.2:c.*116C>G	NP_001298240.1:n.*116C>G
NM_206824.3:c.*219C>G	NP_996560.1:n.*219C>G