Canonical Allele Identifier: CA400860610
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171625T>A (hg19) chr17:g.70175484T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175484T>A , CM000679.2:g.70175484T>A GRCh38
NC_000017.10:g.68171625T>A , CM000679.1:g.68171625T>A GRCh37
NC_000017.9:g.65683220T>A NCBI36
NG_008798.1:g.10950T>A , LRG_328:g.10950T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.445T>A MANE Select ENSP00000243457.2:p.Cys149Ser
ENST00000243457.3:c.445T>A ENSP00000243457.2:p.Cys149Ser
ENST00000535240.1:c.445T>A ENSP00000441848.1:p.Cys149Ser
NM_000891.2:c.445T>A , LRG_328t1:c.445T>A NP_000882.1:p.Cys149Ser
XM_011524779.1:c.445T>A XP_011523081.1:p.Cys149Ser
NM_000891.3:c.445T>A MANE Select NP_000882.1:p.Cys149Ser
Search 100 bp 5'
Search 100 bp 3'