Canonical Allele Identifier: CA501700909

Gene: KCNJ2

Linked Data

• MyVariant Identifiers: chr17:g.68172149C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.70176008C>T , CM000679.2:g.70176008C>T	GRCh38
NC_000017.10:g.68172149C>T , CM000679.1:g.68172149C>T	GRCh37
NC_000017.9:g.65683744C>T	NCBI36
NG_008798.1:g.11474C>T , LRG_328:g.11474C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000243457.4:c.969C>T MANE Select	ENSP00000243457.2:p.Gly323=
ENST00000243457.3:c.969C>T	ENSP00000243457.2:p.Gly323=
ENST00000535240.1:c.969C>T	ENSP00000441848.1:p.Gly323=
NM_000891.2:c.969C>T , LRG_328t1:c.969C>T	NP_000882.1:p.Gly323=
XM_011524779.1:c.969C>T	XP_011523081.1:p.Gly323=
NM_000891.3:c.969C>T MANE Select	NP_000882.1:p.Gly323=