Canonical Allele Identifier: CA2668886399
Gene: EHHADH HGNC NCBI

Linked Data

gnomAD v4: 3-185254202-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254202C>T , CM000665.2:g.185254202C>T GRCh38
NC_000003.11:g.184971990C>T , CM000665.1:g.184971990C>T GRCh37
NC_000003.10:g.186454684C>T NCBI36
NG_015999.1:g.4897G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5685G>A
XM_011512517.1:c.-214-5685G>A XP_011510819.1:n.-214-5685G>A
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