Canonical Allele Identifier: CA293703015
Gene: KCNJ2 HGNC NCBI

Linked Data

dbSNP Id: rs916453232
gnomAD v3: 17-70177102-G-A
gnomAD v4: 17-70177102-G-A
MyVariant Identifiers: chr17:g.68173243G>A (hg19) chr17:g.70177102G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70177102G>A , CM000679.2:g.70177102G>A GRCh38
NC_000017.10:g.68173243G>A , CM000679.1:g.68173243G>A GRCh37
NC_000017.9:g.65684838G>A NCBI36
NG_008798.1:g.12568G>A , LRG_328:g.12568G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.*779G>A MANE Select ENSP00000243457.2:n.*779G>A
ENST00000243457.3:c.*779G>A ENSP00000243457.2:n.*779G>A
NM_000891.2:c.*779G>A , LRG_328t1:c.*779G>A NP_000882.1:n.*779G>A
XM_011524779.1:c.*779G>A XP_011523081.1:n.*779G>A
NM_000891.3:c.*779G>A MANE Select NP_000882.1:n.*779G>A
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