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Canonical Allele Identifier:
CA410196249
Gene: KCNE2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr21:g.35742862A>C (hg19)
chr21:g.34370563A>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.34370563A>C , CM000683.2:g.34370563A>C
GRCh38
NC_000021.8:g.35742862A>C , CM000683.1:g.35742862A>C
GRCh37
NC_000021.7:g.34664732A>C
NCBI36
NG_008804.1:g.11540A>C , LRG_291:g.11540A>C
Transcript Alleles
HGVS
Amino-acid change
NM_172201.1:c.85A>C , LRG_291t1:c.85A>C
NP_751951.1:p.Asn29His
XR_937683.1:n.758T>G
XR_937684.1:n.758T>G
XR_001755012.2:n.879T>G
XR_001755013.2:n.758T>G
XR_937683.2:n.758T>G
NM_172201.2:c.85A>C
NP_751951.1:p.Asn29His
ENST00000290310.3:c.85A>C
ENSP00000290310.2:p.Asn29His
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