Canonical Allele Identifier: CA400861785
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171899G>T (hg19) chr17:g.70175758G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175758G>T , CM000679.2:g.70175758G>T GRCh38
NC_000017.10:g.68171899G>T , CM000679.1:g.68171899G>T GRCh37
NC_000017.9:g.65683494G>T NCBI36
NG_008798.1:g.11224G>T , LRG_328:g.11224G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.719G>T MANE Select ENSP00000243457.2:p.Gly240Val
ENST00000243457.3:c.719G>T ENSP00000243457.2:p.Gly240Val
ENST00000535240.1:c.719G>T ENSP00000441848.1:p.Gly240Val
NM_000891.2:c.719G>T , LRG_328t1:c.719G>T NP_000882.1:p.Gly240Val
XM_011524779.1:c.719G>T XP_011523081.1:p.Gly240Val
NM_000891.3:c.719G>T MANE Select NP_000882.1:p.Gly240Val
Search 100 bp 5'
Search 100 bp 3'