Canonical Allele Identifier: CA1426396733
Gene: EHHADH HGNC NCBI

Linked Data

dbSNP Id: rs1719840803

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254318G>A , CM000665.2:g.185254318G>A GRCh38
NC_000003.11:g.184972106G>A , CM000665.1:g.184972106G>A GRCh37
NC_000003.10:g.186454800G>A NCBI36
NG_015999.1:g.4781C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5801C>T
XM_011512517.1:c.-214-5801C>T XP_011510819.1:n.-214-5801C>T