Canonical Allele Identifier: CA2668886379
Gene: EHHADH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254188del , CM000665.2:g.185254188del GRCh38
NC_000003.11:g.184971976del , CM000665.1:g.184971976del GRCh37
NC_000003.10:g.186454670del NCBI36
NG_015999.1:g.4914del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5668del
XM_011512517.1:c.-214-5668del XP_011510819.1:n.-214-5668del