Canonical Allele Identifier: CA501700798
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171699T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175558T>A , CM000679.2:g.70175558T>A GRCh38
NC_000017.10:g.68171699T>A , CM000679.1:g.68171699T>A GRCh37
NC_000017.9:g.65683294T>A NCBI36
NG_008798.1:g.11024T>A , LRG_328:g.11024T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.519T>A MANE Select ENSP00000243457.2:p.Ala173=
ENST00000243457.3:c.519T>A ENSP00000243457.2:p.Ala173=
ENST00000535240.1:c.519T>A ENSP00000441848.1:p.Ala173=
NM_000891.2:c.519T>A , LRG_328t1:c.519T>A NP_000882.1:p.Ala173=
XM_011524779.1:c.519T>A XP_011523081.1:p.Ala173=
NM_000891.3:c.519T>A MANE Select NP_000882.1:p.Ala173=