Canonical Allele Identifier: CA1253627663

Gene: VRK2

Linked Data

• dbSNP Id: rs1672406009

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.57980969C>A , CM000664.2:g.57980969C>A	GRCh38
NC_000002.11:g.58208104C>A , CM000664.1:g.58208104C>A	GRCh37
NC_000002.10:g.58061608C>A	NCBI36
NG_029717.2:g.78229C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000648897.1:c.-728-37047C>A	ENSP00000497378.1:n.-728-37047C>A
ENST00000417641.6:c.-438-44696C>A	ENSP00000402375.2:n.-438-44696C>A
ENST00000435505.6:c.-556-44696C>A	ENSP00000408002.2:n.-556-44696C>A
ENST00000463222.1:n.185-44696C>A
ENST00000478687.5:n.189-37047C>A
NM_001288837.1:c.-556-44696C>A	NP_001275766.1:n.-556-44696C>A
NM_001288838.1:c.-438-44696C>A	NP_001275767.1:n.-438-44696C>A
XR_940118.1:n.241-43835G>T
XR_940119.1:n.241-43835G>T
XR_940120.1:n.214-43835G>T
XR_940121.1:n.355-43835G>T
XR_940122.1:n.250-43835G>T
NM_001288837.2:c.-556-44696C>A	NP_001275766.1:n.-556-44696C>A
NM_001288838.2:c.-438-44696C>A	NP_001275767.1:n.-438-44696C>A