Canonical Allele Identifier: CA501700544
Gene: KCNJ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.68171745A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70175604A>C , CM000679.2:g.70175604A>C GRCh38
NC_000017.10:g.68171745A>C , CM000679.1:g.68171745A>C GRCh37
NC_000017.9:g.65683340A>C NCBI36
NG_008798.1:g.11070A>C , LRG_328:g.11070A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243457.4:c.565A>C MANE Select ENSP00000243457.2:p.Arg189=
ENST00000243457.3:c.565A>C ENSP00000243457.2:p.Arg189=
ENST00000535240.1:c.565A>C ENSP00000441848.1:p.Arg189=
NM_000891.2:c.565A>C , LRG_328t1:c.565A>C NP_000882.1:p.Arg189=
XM_011524779.1:c.565A>C XP_011523081.1:p.Arg189=
NM_000891.3:c.565A>C MANE Select NP_000882.1:p.Arg189=