Canonical Allele Identifier: CA501700627
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171609A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175468A>C , CM000679.2:g.70175468A>C GRCh38
NC_000017.10:g.68171609A>C , CM000679.1:g.68171609A>C GRCh37
NC_000017.9:g.65683204A>C NCBI36
NG_008798.1:g.10934A>C , LRG_328:g.10934A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.429A>C MANE Select ENSP00000243457.2:p.Ile143=
ENST00000243457.3:c.429A>C ENSP00000243457.2:p.Ile143=
ENST00000535240.1:c.429A>C ENSP00000441848.1:p.Ile143=
NM_000891.2:c.429A>C , LRG_328t1:c.429A>C NP_000882.1:p.Ile143=
XM_011524779.1:c.429A>C XP_011523081.1:p.Ile143=
NM_000891.3:c.429A>C MANE Select NP_000882.1:p.Ile143=