Canonical Allele Identifier: CA512298917
Gene: KCNE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.35743246T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370947T>A , CM000683.2:g.34370947T>A GRCh38
NC_000021.8:g.35743246T>A , CM000683.1:g.35743246T>A GRCh37
NC_000021.7:g.34665116T>A NCBI36
NG_008804.1:g.11924T>A , LRG_291:g.11924T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290310.4:c.*97T>A MANE Select ENSP00000290310.2:n.*97T>A
ENST00000290310.3:c.*97T>A ENSP00000290310.2:n.*97T>A
NM_172201.1:c.*97T>A , LRG_291t1:c.*97T>A NP_751951.1:n.*97T>A
XR_937683.1:n.374A>T
XR_937684.1:n.374A>T
XR_001755012.2:n.495A>T
XR_001755013.2:n.374A>T
XR_937683.2:n.374A>T
NM_172201.2:c.*97T>A MANE Select NP_751951.1:n.*97T>A