Canonical Allele Identifier: CA329714
Gene: KCNJ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67593
dbSNP Id: rs199473388

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175965C>T , CM000679.2:g.70175965C>T GRCh38
NC_000017.10:g.68172106C>T , CM000679.1:g.68172106C>T GRCh37
NC_000017.9:g.65683701C>T NCBI36
NG_008798.1:g.11431C>T , LRG_328:g.11431C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000243457.4:c.926C>T MANE Select ENSP00000243457.2:p.Thr309Ile
ENST00000243457.3:c.926C>T ENSP00000243457.2:p.Thr309Ile
ENST00000535240.1:c.926C>T ENSP00000441848.1:p.Thr309Ile
NM_000891.2:c.926C>T , LRG_328t1:c.926C>T NP_000882.1:p.Thr309Ile
XM_011524779.1:c.926C>T XP_011523081.1:p.Thr309Ile
NM_000891.3:c.926C>T MANE Select NP_000882.1:p.Thr309Ile