Canonical Allele Identifier: CA1426396673
Gene: EHHADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254182A= , CM000665.2:g.185254182A= GRCh38
NC_000003.11:g.184971970A= , CM000665.1:g.184971970A= GRCh37
NC_000003.10:g.186454664A= NCBI36
NG_015999.1:g.4917T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5665T=
XM_011512517.1:c.-214-5665T= XP_011510819.1:n.-214-5665T=