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Canonical Allele Identifier:
CA410196589
Gene: KCNE2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr21:g.35742962T>A (hg19)
chr21:g.34370663T>A (hg38)
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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
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
NP_751951.1:p.Phe62Tyr
ENST00000290310.3:c.185T>A
ENSP00000290310.2:p.Phe62Tyr
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