Canonical Allele Identifier: CA400860636

Gene: KCNJ2

Linked Data

• dbSNP Id: rs2074387261
• MyVariant Identifiers: chr17:g.68171636T>G (hg19) ; chr17:g.70175495T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.70175495T>G , CM000679.2:g.70175495T>G	GRCh38
NC_000017.10:g.68171636T>G , CM000679.1:g.68171636T>G	GRCh37
NC_000017.9:g.65683231T>G	NCBI36
NG_008798.1:g.10961T>G , LRG_328:g.10961T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243457.4:c.456T>G MANE Select	ENSP00000243457.2:p.Asp152Glu
ENST00000243457.3:c.456T>G	ENSP00000243457.2:p.Asp152Glu
ENST00000535240.1:c.456T>G	ENSP00000441848.1:p.Asp152Glu
NM_000891.2:c.456T>G , LRG_328t1:c.456T>G	NP_000882.1:p.Asp152Glu
XM_011524779.1:c.456T>G	XP_011523081.1:p.Asp152Glu
NM_000891.3:c.456T>G MANE Select	NP_000882.1:p.Asp152Glu