Canonical Allele Identifier: CA774609397
Gene: KCNJ2 HGNC NCBI

Linked Data

dbSNP Id: rs1159936034
MyVariant Identifiers: chr17:g.68175547T>A (hg19) chr17:g.70179406T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70179406T>A , CM000679.2:g.70179406T>A GRCh38
NC_000017.10:g.68175547T>A , CM000679.1:g.68175547T>A GRCh37
NC_000017.9:g.65687142T>A NCBI36
NG_008798.1:g.14872T>A , LRG_328:g.14872T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.*3083T>A MANE Select ENSP00000243457.2:n.*3083T>A
ENST00000243457.3:c.*3083T>A ENSP00000243457.2:n.*3083T>A
NM_000891.2:c.*3083T>A , LRG_328t1:c.*3083T>A NP_000882.1:n.*3083T>A
NM_000891.3:c.*3083T>A MANE Select NP_000882.1:n.*3083T>A
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