Canonical Allele Identifier: CA512298915
Gene: KCNE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.35743246T>G (hg19)
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Genomic Alleles

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

Transcript Alleles

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