Canonical Allele Identifier: CA400861159
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171770A>C (hg19) chr17:g.70175629A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175629A>C , CM000679.2:g.70175629A>C GRCh38
NC_000017.10:g.68171770A>C , CM000679.1:g.68171770A>C GRCh37
NC_000017.9:g.65683365A>C NCBI36
NG_008798.1:g.11095A>C , LRG_328:g.11095A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.590A>C MANE Select ENSP00000243457.2:p.His197Pro
ENST00000243457.3:c.590A>C ENSP00000243457.2:p.His197Pro
ENST00000535240.1:c.590A>C ENSP00000441848.1:p.His197Pro
NM_000891.2:c.590A>C , LRG_328t1:c.590A>C NP_000882.1:p.His197Pro
XM_011524779.1:c.590A>C XP_011523081.1:p.His197Pro
NM_000891.3:c.590A>C MANE Select NP_000882.1:p.His197Pro
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