Canonical Allele Identifier: CA1426396689
Gene: EHHADH HGNC NCBI

Linked Data

dbSNP Id: rs1719837899

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254222_185254245del , CM000665.2:g.185254222_185254245del GRCh38
NC_000003.11:g.184972010_184972033del , CM000665.1:g.184972010_184972033del GRCh37
NC_000003.10:g.186454704_186454727del NCBI36
NG_015999.1:g.4858_4881del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5724_228-5701del
XM_011512517.1:c.-214-5724_-214-5701del XP_011510819.1:n.-214-5724_-214-5701del