Canonical Allele Identifier: CA10013432
Gene: KCNE2 HGNC NCBI

Linked Data

dbSNP Id: rs771699510

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370740A>C , CM000683.2:g.34370740A>C GRCh38
NC_000021.8:g.35743039A>C , CM000683.1:g.35743039A>C GRCh37
NC_000021.7:g.34664909A>C NCBI36
NG_008804.1:g.11717A>C , LRG_291:g.11717A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290310.4:c.262A>C MANE Select ENSP00000290310.2:p.Ile88Leu
ENST00000290310.3:c.262A>C ENSP00000290310.2:p.Ile88Leu
NM_172201.1:c.262A>C , LRG_291t1:c.262A>C NP_751951.1:p.Ile88Leu
XR_937683.1:n.581T>G
XR_937684.1:n.581T>G
XR_001755012.2:n.702T>G
XR_001755013.2:n.581T>G
XR_937683.2:n.581T>G
NM_172201.2:c.262A>C MANE Select NP_751951.1:p.Ile88Leu