Canonical Allele Identifier: CA1426396749
Gene: EHHADH HGNC NCBI

Linked Data

dbSNP Id: rs1391798824

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254348T>G , CM000665.2:g.185254348T>G GRCh38
NC_000003.11:g.184972136T>G , CM000665.1:g.184972136T>G GRCh37
NC_000003.10:g.186454830T>G NCBI36
NG_015999.1:g.4751A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5831A>C
XM_011512517.1:c.-214-5831A>C XP_011510819.1:n.-214-5831A>C