Canonical Allele Identifier: CA89521547
Gene: EHHADH HGNC NCBI

Linked Data

dbSNP Id: rs539033113
gnomAD v2: 3-184971888-AGAG-A
gnomAD v3: 3-185254100-AGAG-A
gnomAD v4: 3-185254100-AGAG-A
MyVariant Identifiers: chr3:g.184971889_184971891del (hg19) chr3:g.185254101_185254103del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254105_185254107del , CM000665.2:g.185254105_185254107del GRCh38
NC_000003.11:g.184971893_184971895del , CM000665.1:g.184971893_184971895del GRCh37
NC_000003.10:g.186454587_186454589del NCBI36
NG_015999.1:g.4996_4998del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5586_228-5584del
XM_011512517.1:c.-214-5586_-214-5584del XP_011510819.1:n.-214-5586_-214-5584del
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