Canonical Allele Identifier: CA2668886292
Gene: EHHADH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254127dup , CM000665.2:g.185254127dup GRCh38
NC_000003.11:g.184971915dup , CM000665.1:g.184971915dup GRCh37
NC_000003.10:g.186454609dup NCBI36
NG_015999.1:g.4972dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5610dup
XM_011512517.1:c.-214-5610dup XP_011510819.1:n.-214-5610dup