Canonical Allele Identifier: CA501700728

Gene: KCNJ2

Linked Data

• dbSNP Id: rs1231353264
• MyVariant Identifiers: chr17:g.68171663G>A (hg19) ; chr17:g.70175522G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.70175522G>A , CM000679.2:g.70175522G>A	GRCh38
NC_000017.10:g.68171663G>A , CM000679.1:g.68171663G>A	GRCh37
NC_000017.9:g.65683258G>A	NCBI36
NG_008798.1:g.10988G>A , LRG_328:g.10988G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243457.4:c.483G>A MANE Select	ENSP00000243457.2:p.Val161=
ENST00000243457.3:c.483G>A	ENSP00000243457.2:p.Val161=
ENST00000535240.1:c.483G>A	ENSP00000441848.1:p.Val161=
NM_000891.2:c.483G>A , LRG_328t1:c.483G>A	NP_000882.1:p.Val161=
XM_011524779.1:c.483G>A	XP_011523081.1:p.Val161=
NM_000891.3:c.483G>A MANE Select	NP_000882.1:p.Val161=