Canonical Allele Identifier: CA774609371
Gene: KCNJ2 HGNC NCBI

Linked Data

dbSNP Id: rs1391888381
MyVariant Identifiers: chr17:g.68175515G>T (hg19) chr17:g.70179374G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70179374G>T , CM000679.2:g.70179374G>T GRCh38
NC_000017.10:g.68175515G>T , CM000679.1:g.68175515G>T GRCh37
NC_000017.9:g.65687110G>T NCBI36
NG_008798.1:g.14840G>T , LRG_328:g.14840G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.*3051G>T MANE Select ENSP00000243457.2:n.*3051G>T
ENST00000243457.3:c.*3051G>T ENSP00000243457.2:n.*3051G>T
NM_000891.2:c.*3051G>T , LRG_328t1:c.*3051G>T NP_000882.1:n.*3051G>T
NM_000891.3:c.*3051G>T MANE Select NP_000882.1:n.*3051G>T
Search 100 bp 5'
Search 100 bp 3'