Canonical Allele Identifier: CA501700683
Gene: KCNJ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2930210
ClinVar RCV Id: RCV003787568
dbSNP Id: rs751862699
MyVariant Identifiers: chr17:g.68171633G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175492G>C , CM000679.2:g.70175492G>C GRCh38
NC_000017.10:g.68171633G>C , CM000679.1:g.68171633G>C GRCh37
NC_000017.9:g.65683228G>C NCBI36
NG_008798.1:g.10958G>C , LRG_328:g.10958G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.453G>C MANE Select ENSP00000243457.2:p.Thr151=
ENST00000243457.3:c.453G>C ENSP00000243457.2:p.Thr151=
ENST00000535240.1:c.453G>C ENSP00000441848.1:p.Thr151=
NM_000891.2:c.453G>C , LRG_328t1:c.453G>C NP_000882.1:p.Thr151=
XM_011524779.1:c.453G>C XP_011523081.1:p.Thr151=
NM_000891.3:c.453G>C MANE Select NP_000882.1:p.Thr151=