Canonical Allele Identifier: CA400861939
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171937G>A (hg19) chr17:g.70175796G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175796G>A , CM000679.2:g.70175796G>A GRCh38
NC_000017.10:g.68171937G>A , CM000679.1:g.68171937G>A GRCh37
NC_000017.9:g.65683532G>A NCBI36
NG_008798.1:g.11262G>A , LRG_328:g.11262G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.757G>A MANE Select ENSP00000243457.2:p.Gly253Arg
ENST00000243457.3:c.757G>A ENSP00000243457.2:p.Gly253Arg
ENST00000535240.1:c.757G>A ENSP00000441848.1:p.Gly253Arg
NM_000891.2:c.757G>A , LRG_328t1:c.757G>A NP_000882.1:p.Gly253Arg
XM_011524779.1:c.757G>A XP_011523081.1:p.Gly253Arg
NM_000891.3:c.757G>A MANE Select NP_000882.1:p.Gly253Arg
Search 100 bp 5'
Search 100 bp 3'