Canonical Allele Identifier: CA2668886247

Gene: EHHADH

Linked Data

• gnomAD v4: 3-185254055-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185254055T>C , CM000665.2:g.185254055T>C	GRCh38
NC_000003.11:g.184971843T>C , CM000665.1:g.184971843T>C	GRCh37
NC_000003.10:g.186454537T>C	NCBI36
NG_015999.1:g.5044A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231887.7:c.-33A>G	ENSP00000231887.3:n.-33A>G
ENST00000465178.1:n.228-5538A>G
NM_001166415.1:c.-444A>G	NP_001159887.1:n.-444A>G
NM_001966.3:c.-33A>G	NP_001957.2:n.-33A>G
XM_011512517.1:c.-214-5538A>G	XP_011510819.1:n.-214-5538A>G