Canonical Allele Identifier: CA1253627665
Gene: VRK2 HGNC NCBI

Linked Data

dbSNP Id: rs1672406090
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.57980971T>C , CM000664.2:g.57980971T>C GRCh38
NC_000002.11:g.58208106T>C , CM000664.1:g.58208106T>C GRCh37
NC_000002.10:g.58061610T>C NCBI36
NG_029717.2:g.78231T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648897.1:c.-728-37045T>C ENSP00000497378.1:n.-728-37045T>C
ENST00000417641.6:c.-438-44694T>C ENSP00000402375.2:n.-438-44694T>C
ENST00000435505.6:c.-556-44694T>C ENSP00000408002.2:n.-556-44694T>C
ENST00000463222.1:n.185-44694T>C
ENST00000478687.5:n.189-37045T>C
NM_001288837.1:c.-556-44694T>C NP_001275766.1:n.-556-44694T>C
NM_001288838.1:c.-438-44694T>C NP_001275767.1:n.-438-44694T>C
XR_940118.1:n.241-43837A>G
XR_940119.1:n.241-43837A>G
XR_940120.1:n.214-43837A>G
XR_940121.1:n.355-43837A>G
XR_940122.1:n.250-43837A>G
NM_001288837.2:c.-556-44694T>C NP_001275766.1:n.-556-44694T>C
NM_001288838.2:c.-438-44694T>C NP_001275767.1:n.-438-44694T>C
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