Canonical Allele Identifier: CA774609431
Gene: KCNJ2 HGNC NCBI

Linked Data

dbSNP Id: rs1269178333
MyVariant Identifiers: chr17:g.68175595A>G (hg19) chr17:g.70179454A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70179454A>G , CM000679.2:g.70179454A>G GRCh38
NC_000017.10:g.68175595A>G , CM000679.1:g.68175595A>G GRCh37
NC_000017.9:g.65687190A>G NCBI36
NG_008798.1:g.14920A>G , LRG_328:g.14920A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.*3131A>G MANE Select ENSP00000243457.2:n.*3131A>G
ENST00000243457.3:c.*3131A>G ENSP00000243457.2:n.*3131A>G
NM_000891.2:c.*3131A>G , LRG_328t1:c.*3131A>G NP_000882.1:n.*3131A>G
NM_000891.3:c.*3131A>G MANE Select NP_000882.1:n.*3131A>G
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