Canonical Allele Identifier: CA2272996419
Gene: KCNJ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175078T= , CM000679.2:g.70175078T= GRCh38
NC_000017.10:g.68171219T= , CM000679.1:g.68171219T= GRCh37
NC_000017.9:g.65682814T= NCBI36
NG_008798.1:g.10544T= , LRG_328:g.10544T=

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.39T= MANE Select ENSP00000243457.2:p.Ser13=
ENST00000243457.3:c.39T= ENSP00000243457.2:p.Ser13=
ENST00000535240.1:c.39T= ENSP00000441848.1:p.Ser13=
NM_000891.2:c.39T= , LRG_328t1:c.39T= NP_000882.1:p.Ser13=
XM_011524779.1:c.39T= XP_011523081.1:p.Ser13=
NM_000891.3:c.39T= MANE Select NP_000882.1:p.Ser13=