Canonical Allele Identifier: CA10013395
Gene: KCNE2 HGNC NCBI

Linked Data

dbSNP Id: rs775857492

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370544T>C , CM000683.2:g.34370544T>C GRCh38
NC_000021.8:g.35742843T>C , CM000683.1:g.35742843T>C GRCh37
NC_000021.7:g.34664713T>C NCBI36
NG_008804.1:g.11521T>C , LRG_291:g.11521T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290310.4:c.66T>C MANE Select ENSP00000290310.2:p.Tyr22=
ENST00000290310.3:c.66T>C ENSP00000290310.2:p.Tyr22=
NM_172201.1:c.66T>C , LRG_291t1:c.66T>C NP_751951.1:p.Tyr22=
XR_937683.1:n.777A>G
XR_937684.1:n.777A>G
XR_001755012.2:n.898A>G
XR_001755013.2:n.777A>G
XR_937683.2:n.777A>G
NM_172201.2:c.66T>C MANE Select NP_751951.1:p.Tyr22=