Canonical Allele Identifier: CA1426396680
Gene: EHHADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254205A= , CM000665.2:g.185254205A= GRCh38
NC_000003.11:g.184971993A= , CM000665.1:g.184971993A= GRCh37
NC_000003.10:g.186454687A= NCBI36
NG_015999.1:g.4894T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5688T=
XM_011512517.1:c.-214-5688T= XP_011510819.1:n.-214-5688T=