Canonical Allele Identifier: CA1426396665
Gene: EHHADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254169C= , CM000665.2:g.185254169C= GRCh38
NC_000003.11:g.184971957C= , CM000665.1:g.184971957C= GRCh37
NC_000003.10:g.186454651C= NCBI36
NG_015999.1:g.4930G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5652G=
XM_011512517.1:c.-214-5652G= XP_011510819.1:n.-214-5652G=