Canonical Allele Identifier: CA501700669

Gene: KCNJ2

Linked Data

• dbSNP Id: rs1215177873
• MyVariant Identifiers: chr17:g.68171627T>C (hg19) ; chr17:g.70175486T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.70175486T>C , CM000679.2:g.70175486T>C	GRCh38
NC_000017.10:g.68171627T>C , CM000679.1:g.68171627T>C	GRCh37
NC_000017.9:g.65683222T>C	NCBI36
NG_008798.1:g.10952T>C , LRG_328:g.10952T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243457.4:c.447T>C MANE Select	ENSP00000243457.2:p.Cys149=
ENST00000243457.3:c.447T>C	ENSP00000243457.2:p.Cys149=
ENST00000535240.1:c.447T>C	ENSP00000441848.1:p.Cys149=
NM_000891.2:c.447T>C , LRG_328t1:c.447T>C	NP_000882.1:p.Cys149=
XM_011524779.1:c.447T>C	XP_011523081.1:p.Cys149=
NM_000891.3:c.447T>C MANE Select	NP_000882.1:p.Cys149=