Canonical Allele Identifier: CA410196589
Gene: KCNE2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370663T>A , CM000683.2:g.34370663T>A GRCh38
NC_000021.8:g.35742962T>A , CM000683.1:g.35742962T>A GRCh37
NC_000021.7:g.34664832T>A NCBI36
NG_008804.1:g.11640T>A , LRG_291:g.11640T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290310.4:c.185T>A MANE Select ENSP00000290310.2:p.Phe62Tyr
ENST00000290310.3:c.185T>A ENSP00000290310.2:p.Phe62Tyr
NM_172201.1:c.185T>A , LRG_291t1:c.185T>A NP_751951.1:p.Phe62Tyr
XR_937683.1:n.658A>T
XR_937684.1:n.658A>T
XR_001755012.2:n.779A>T
XR_001755013.2:n.658A>T
XR_937683.2:n.658A>T
NM_172201.2:c.185T>A MANE Select NP_751951.1:p.Phe62Tyr