Canonical Allele Identifier: CA774607439
Gene: KCNJ2 HGNC NCBI

Linked Data

dbSNP Id: rs1301344296

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70177233T>G , CM000679.2:g.70177233T>G GRCh38
NC_000017.10:g.68173374T>G , CM000679.1:g.68173374T>G GRCh37
NC_000017.9:g.65684969T>G NCBI36
NG_008798.1:g.12699T>G , LRG_328:g.12699T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.*910T>G MANE Select ENSP00000243457.2:n.*910T>G
ENST00000243457.3:c.*910T>G ENSP00000243457.2:n.*910T>G
NM_000891.2:c.*910T>G , LRG_328t1:c.*910T>G NP_000882.1:n.*910T>G
XM_011524779.1:c.*910T>G XP_011523081.1:n.*910T>G
NM_000891.3:c.*910T>G MANE Select NP_000882.1:n.*910T>G