Canonical Allele Identifier: CA2272996581
Gene: KCNJ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175492G= , CM000679.2:g.70175492G= GRCh38
NC_000017.10:g.68171633G= , CM000679.1:g.68171633G= GRCh37
NC_000017.9:g.65683228G= NCBI36
NG_008798.1:g.10958G= , LRG_328:g.10958G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.453G= MANE Select ENSP00000243457.2:p.Thr151=
ENST00000243457.3:c.453G= ENSP00000243457.2:p.Thr151=
ENST00000535240.1:c.453G= ENSP00000441848.1:p.Thr151=
NM_000891.2:c.453G= , LRG_328t1:c.453G= NP_000882.1:p.Thr151=
XM_011524779.1:c.453G= XP_011523081.1:p.Thr151=
NM_000891.3:c.453G= MANE Select NP_000882.1:p.Thr151=