Canonical Allele Identifier: CA48720645

Gene: VRK2

Linked Data

• dbSNP Id: rs554478600
• MyVariant Identifiers: chr2:g.58208083G>C (hg19) ; chr2:g.57980948G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.57980948G>C , CM000664.2:g.57980948G>C	GRCh38
NC_000002.11:g.58208083G>C , CM000664.1:g.58208083G>C	GRCh37
NC_000002.10:g.58061587G>C	NCBI36
NG_029717.2:g.78208G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000648897.1:c.-728-37068G>C	ENSP00000497378.1:n.-728-37068G>C
ENST00000417641.6:c.-438-44717G>C	ENSP00000402375.2:n.-438-44717G>C
ENST00000435505.6:c.-556-44717G>C	ENSP00000408002.2:n.-556-44717G>C
ENST00000463222.1:n.185-44717G>C
ENST00000478687.5:n.189-37068G>C
NM_001288837.1:c.-556-44717G>C	NP_001275766.1:n.-556-44717G>C
NM_001288838.1:c.-438-44717G>C	NP_001275767.1:n.-438-44717G>C
XR_940118.1:n.241-43814C>G
XR_940119.1:n.241-43814C>G
XR_940120.1:n.214-43814C>G
XR_940121.1:n.355-43814C>G
XR_940122.1:n.250-43814C>G
NM_001288837.2:c.-556-44717G>C	NP_001275766.1:n.-556-44717G>C
NM_001288838.2:c.-438-44717G>C	NP_001275767.1:n.-438-44717G>C