Canonical Allele Identifier: CA2704891647
Gene: EHHADH HGNC NCBI

Linked Data

dbSNP Id: rs2108656072

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254282C>G , CM000665.2:g.185254282C>G GRCh38
NC_000003.11:g.184972070C>G , CM000665.1:g.184972070C>G GRCh37
NC_000003.10:g.186454764C>G NCBI36
NG_015999.1:g.4817G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5765G>C
XM_011512517.1:c.-214-5765G>C XP_011510819.1:n.-214-5765G>C