Canonical Allele Identifier: CA329675
Gene: KCNJ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67576
dbSNP Id: rs199473654

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175475G>A , CM000679.2:g.70175475G>A GRCh38
NC_000017.10:g.68171616G>A , CM000679.1:g.68171616G>A GRCh37
NC_000017.9:g.65683211G>A NCBI36
NG_008798.1:g.10941G>A , LRG_328:g.10941G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.436G>A MANE Select ENSP00000243457.2:p.Gly146Ser
ENST00000243457.3:c.436G>A ENSP00000243457.2:p.Gly146Ser
ENST00000535240.1:c.436G>A ENSP00000441848.1:p.Gly146Ser
NM_000891.2:c.436G>A , LRG_328t1:c.436G>A NP_000882.1:p.Gly146Ser
XM_011524779.1:c.436G>A XP_011523081.1:p.Gly146Ser
NM_000891.3:c.436G>A MANE Select NP_000882.1:p.Gly146Ser