Canonical Allele Identifier: CA1057301837
Gene: EHHADH HGNC NCBI

Linked Data

dbSNP Id: rs1719835562

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254138G>A , CM000665.2:g.185254138G>A GRCh38
NC_000003.11:g.184971926G>A , CM000665.1:g.184971926G>A GRCh37
NC_000003.10:g.186454620G>A NCBI36
NG_015999.1:g.4961C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5621C>T
XM_011512517.1:c.-214-5621C>T XP_011510819.1:n.-214-5621C>T