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Canonical Allele Identifier:
CA410196251
Gene: KCNE2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr21:g.35742862A>T (hg19)
chr21:g.34370563A>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.34370563A>T , CM000683.2:g.34370563A>T
GRCh38
NC_000021.8:g.35742862A>T , CM000683.1:g.35742862A>T
GRCh37
NC_000021.7:g.34664732A>T
NCBI36
NG_008804.1:g.11540A>T , LRG_291:g.11540A>T
Transcript Alleles
HGVS
Amino-acid change
NM_172201.1:c.85A>T , LRG_291t1:c.85A>T
NP_751951.1:p.Asn29Tyr
XR_937683.1:n.758T>A
XR_937684.1:n.758T>A
XR_001755012.2:n.879T>A
XR_001755013.2:n.758T>A
XR_937683.2:n.758T>A
NM_172201.2:c.85A>T
NP_751951.1:p.Asn29Tyr
ENST00000290310.3:c.85A>T
ENSP00000290310.2:p.Asn29Tyr
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