Canonical Allele Identifier: CA10649967
Gene: KCNJ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 324847
dbSNP Id: rs10083831

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70177155G>A , CM000679.2:g.70177155G>A GRCh38
NC_000017.10:g.68173296G>A , CM000679.1:g.68173296G>A GRCh37
NC_000017.9:g.65684891G>A NCBI36
NG_008798.1:g.12621G>A , LRG_328:g.12621G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.*832G>A MANE Select ENSP00000243457.2:n.*832G>A
ENST00000243457.3:c.*832G>A ENSP00000243457.2:n.*832G>A
NM_000891.2:c.*832G>A , LRG_328t1:c.*832G>A NP_000882.1:n.*832G>A
XM_011524779.1:c.*832G>A XP_011523081.1:n.*832G>A
NM_000891.3:c.*832G>A MANE Select NP_000882.1:n.*832G>A