Canonical Allele Identifier: CA1426396655

Gene: EHHADH

Linked Data

• dbSNP Id: rs1719835999

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185254147C>T , CM000665.2:g.185254147C>T	GRCh38
NC_000003.11:g.184971935C>T , CM000665.1:g.184971935C>T	GRCh37
NC_000003.10:g.186454629C>T	NCBI36
NG_015999.1:g.4952G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465178.1:n.228-5630G>A
XM_011512517.1:c.-214-5630G>A	XP_011510819.1:n.-214-5630G>A