Canonical Allele Identifier: CA770608080

Gene: VRK2

Linked Data

• dbSNP Id: rs1240494395
• gnomAD v3: 2-57980957-A-G
• gnomAD v4: 2-57980957-A-G
• MyVariant Identifiers: chr2:g.58208092A>G (hg19) ; chr2:g.57980957A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.57980957A>G , CM000664.2:g.57980957A>G	GRCh38
NC_000002.11:g.58208092A>G , CM000664.1:g.58208092A>G	GRCh37
NC_000002.10:g.58061596A>G	NCBI36
NG_029717.2:g.78217A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000648897.1:c.-728-37059A>G	ENSP00000497378.1:n.-728-37059A>G
ENST00000417641.6:c.-438-44708A>G	ENSP00000402375.2:n.-438-44708A>G
ENST00000435505.6:c.-556-44708A>G	ENSP00000408002.2:n.-556-44708A>G
ENST00000463222.1:n.185-44708A>G
ENST00000478687.5:n.189-37059A>G
NM_001288837.1:c.-556-44708A>G	NP_001275766.1:n.-556-44708A>G
NM_001288838.1:c.-438-44708A>G	NP_001275767.1:n.-438-44708A>G
XR_940118.1:n.241-43823T>C
XR_940119.1:n.241-43823T>C
XR_940120.1:n.214-43823T>C
XR_940121.1:n.355-43823T>C
XR_940122.1:n.250-43823T>C
NM_001288837.2:c.-556-44708A>G	NP_001275766.1:n.-556-44708A>G
NM_001288838.2:c.-438-44708A>G	NP_001275767.1:n.-438-44708A>G