Canonical Allele Identifier: CA501700469
Gene: KCNJ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1301226
ClinVar RCV Id: RCV001733297
dbSNP Id: rs2074386028
MyVariant Identifiers: chr17:g.68171447C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175306C>T , CM000679.2:g.70175306C>T GRCh38
NC_000017.10:g.68171447C>T , CM000679.1:g.68171447C>T GRCh37
NC_000017.9:g.65683042C>T NCBI36
NG_008798.1:g.10772C>T , LRG_328:g.10772C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.267C>T MANE Select ENSP00000243457.2:p.Cys89=
ENST00000243457.3:c.267C>T ENSP00000243457.2:p.Cys89=
ENST00000535240.1:c.267C>T ENSP00000441848.1:p.Cys89=
NM_000891.2:c.267C>T , LRG_328t1:c.267C>T NP_000882.1:p.Cys89=
XM_011524779.1:c.267C>T XP_011523081.1:p.Cys89=
NM_000891.3:c.267C>T MANE Select NP_000882.1:p.Cys89=