Canonical Allele Identifier: CA302046
Gene: KCNJ2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 67587
dbSNP Id: rs199473385

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175818G>C , CM000679.2:g.70175818G>C GRCh38
NC_000017.10:g.68171959G>C , CM000679.1:g.68171959G>C GRCh37
NC_000017.9:g.65683554G>C NCBI36
NG_008798.1:g.11284G>C , LRG_328:g.11284G>C

Transcript Alleles

HGVS Amino-acid change
NM_000891.2:c.779G>C , LRG_328t1:c.779G>C NP_000882.1:p.Arg260Pro
XM_011524779.1:c.779G>C XP_011523081.1:p.Arg260Pro
ENST00000243457.3:c.779G>C ENSP00000243457.2:p.Arg260Pro
ENST00000535240.1:c.779G>C ENSP00000441848.1:p.Arg260Pro