Canonical Allele Identifier: CA1426396651
Gene: EHHADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254141G= , CM000665.2:g.185254141G= GRCh38
NC_000003.11:g.184971929G= , CM000665.1:g.184971929G= GRCh37
NC_000003.10:g.186454623G= NCBI36
NG_015999.1:g.4958C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5624C=
XM_011512517.1:c.-214-5624C= XP_011510819.1:n.-214-5624C=