Canonical Allele Identifier: CA2759742112
Gene: EHHADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254172T>A , CM000665.2:g.185254172T>A GRCh38
NC_000003.11:g.184971960T>A , CM000665.1:g.184971960T>A GRCh37
NC_000003.10:g.186454654T>A NCBI36
NG_015999.1:g.4927A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5655A>T
XM_011512517.1:c.-214-5655A>T XP_011510819.1:n.-214-5655A>T