Canonical Allele Identifier: CA2668886291
Gene: EHHADH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254126G>T , CM000665.2:g.185254126G>T GRCh38
NC_000003.11:g.184971914G>T , CM000665.1:g.184971914G>T GRCh37
NC_000003.10:g.186454608G>T NCBI36
NG_015999.1:g.4973C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5609C>A
XM_011512517.1:c.-214-5609C>A XP_011510819.1:n.-214-5609C>A