Canonical Allele Identifier: CA89521579
Gene: EHHADH HGNC NCBI

Linked Data

dbSNP Id: rs952217591

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254286A>C , CM000665.2:g.185254286A>C GRCh38
NC_000003.11:g.184972074A>C , CM000665.1:g.184972074A>C GRCh37
NC_000003.10:g.186454768A>C NCBI36
NG_015999.1:g.4813T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5769T>G
XM_011512517.1:c.-214-5769T>G XP_011510819.1:n.-214-5769T>G