Canonical Allele Identifier: CA1426396732
Gene: EHHADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254316T= , CM000665.2:g.185254316T= GRCh38
NC_000003.11:g.184972104T= , CM000665.1:g.184972104T= GRCh37
NC_000003.10:g.186454798T= NCBI36
NG_015999.1:g.4783A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5799A=
XM_011512517.1:c.-214-5799A= XP_011510819.1:n.-214-5799A=