Canonical Allele Identifier: CA512298953
Gene: KCNE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.35743258T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370959T>A , CM000683.2:g.34370959T>A GRCh38
NC_000021.8:g.35743258T>A , CM000683.1:g.35743258T>A GRCh37
NC_000021.7:g.34665128T>A NCBI36
NG_008804.1:g.11936T>A , LRG_291:g.11936T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290310.4:c.*109T>A MANE Select ENSP00000290310.2:n.*109T>A
ENST00000290310.3:c.*109T>A ENSP00000290310.2:n.*109T>A
NM_172201.1:c.*109T>A , LRG_291t1:c.*109T>A NP_751951.1:n.*109T>A
XR_937683.1:n.362A>T
XR_937684.1:n.362A>T
XR_001755012.2:n.483A>T
XR_001755013.2:n.362A>T
XR_937683.2:n.362A>T
NM_172201.2:c.*109T>A MANE Select NP_751951.1:n.*109T>A