Canonical Allele Identifier: CA400861919
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171932A>T (hg19) chr17:g.70175791A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175791A>T , CM000679.2:g.70175791A>T GRCh38
NC_000017.10:g.68171932A>T , CM000679.1:g.68171932A>T GRCh37
NC_000017.9:g.65683527A>T NCBI36
NG_008798.1:g.11257A>T , LRG_328:g.11257A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.752A>T MANE Select ENSP00000243457.2:p.Asn251Ile
ENST00000243457.3:c.752A>T ENSP00000243457.2:p.Asn251Ile
ENST00000535240.1:c.752A>T ENSP00000441848.1:p.Asn251Ile
NM_000891.2:c.752A>T , LRG_328t1:c.752A>T NP_000882.1:p.Asn251Ile
XM_011524779.1:c.752A>T XP_011523081.1:p.Asn251Ile
NM_000891.3:c.752A>T MANE Select NP_000882.1:p.Asn251Ile
Search 100 bp 5'
Search 100 bp 3'