Canonical Allele Identifier: CA400860829
Gene: KCNJ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175559T>G , CM000679.2:g.70175559T>G GRCh38
NC_000017.10:g.68171700T>G , CM000679.1:g.68171700T>G GRCh37
NC_000017.9:g.65683295T>G NCBI36
NG_008798.1:g.11025T>G , LRG_328:g.11025T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.520T>G MANE Select ENSP00000243457.2:p.Phe174Val
ENST00000243457.3:c.520T>G ENSP00000243457.2:p.Phe174Val
ENST00000535240.1:c.520T>G ENSP00000441848.1:p.Phe174Val
NM_000891.2:c.520T>G , LRG_328t1:c.520T>G NP_000882.1:p.Phe174Val
XM_011524779.1:c.520T>G XP_011523081.1:p.Phe174Val
NM_000891.3:c.520T>G MANE Select NP_000882.1:p.Phe174Val