Canonical Allele Identifier: CA2272996582
Gene: KCNJ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175495T= , CM000679.2:g.70175495T= GRCh38
NC_000017.10:g.68171636T= , CM000679.1:g.68171636T= GRCh37
NC_000017.9:g.65683231T= NCBI36
NG_008798.1:g.10961T= , LRG_328:g.10961T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.456T= MANE Select ENSP00000243457.2:p.Asp152=
ENST00000243457.3:c.456T= ENSP00000243457.2:p.Asp152=
ENST00000535240.1:c.456T= ENSP00000441848.1:p.Asp152=
NM_000891.2:c.456T= , LRG_328t1:c.456T= NP_000882.1:p.Asp152=
XM_011524779.1:c.456T= XP_011523081.1:p.Asp152=
NM_000891.3:c.456T= MANE Select NP_000882.1:p.Asp152=