Canonical Allele Identifier: CA1426396722
Gene: EHHADH HGNC NCBI

Linked Data

dbSNP Id: rs1719839898
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254297A>T , CM000665.2:g.185254297A>T GRCh38
NC_000003.11:g.184972085A>T , CM000665.1:g.184972085A>T GRCh37
NC_000003.10:g.186454779A>T NCBI36
NG_015999.1:g.4802T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5780T>A
XM_011512517.1:c.-214-5780T>A XP_011510819.1:n.-214-5780T>A
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