Canonical Allele Identifier: CA1031099113

Gene: VRK2

Linked Data

• dbSNP Id: rs1672405252
• gnomAD v3: 2-57980941-G-C
• gnomAD v4: 2-57980941-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.57980941G>C , CM000664.2:g.57980941G>C	GRCh38
NC_000002.11:g.58208076G>C , CM000664.1:g.58208076G>C	GRCh37
NC_000002.10:g.58061580G>C	NCBI36
NG_029717.2:g.78201G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000648897.1:c.-728-37075G>C	ENSP00000497378.1:n.-728-37075G>C
ENST00000417641.6:c.-438-44724G>C	ENSP00000402375.2:n.-438-44724G>C
ENST00000435505.6:c.-556-44724G>C	ENSP00000408002.2:n.-556-44724G>C
ENST00000463222.1:n.185-44724G>C
ENST00000478687.5:n.189-37075G>C
NM_001288837.1:c.-556-44724G>C	NP_001275766.1:n.-556-44724G>C
NM_001288838.1:c.-438-44724G>C	NP_001275767.1:n.-438-44724G>C
XR_940118.1:n.241-43807C>G
XR_940119.1:n.241-43807C>G
XR_940120.1:n.214-43807C>G
XR_940121.1:n.355-43807C>G
XR_940122.1:n.250-43807C>G
NM_001288837.2:c.-556-44724G>C	NP_001275766.1:n.-556-44724G>C
NM_001288838.2:c.-438-44724G>C	NP_001275767.1:n.-438-44724G>C