Canonical Allele Identifier: CA2668886319
Gene: EHHADH HGNC NCBI

Linked Data

gnomAD v4: 3-185254142-C-CCCCGG
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254143_185254144insCCGGC , CM000665.2:g.185254143_185254144insCCGGC GRCh38
NC_000003.11:g.184971931_184971932insCCGGC , CM000665.1:g.184971931_184971932insCCGGC GRCh37
NC_000003.10:g.186454625_186454626insCCGGC NCBI36
NG_015999.1:g.4956_4957insCCGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5626_228-5625insCCGGG
XM_011512517.1:c.-214-5626_-214-5625insCCGGG XP_011510819.1:n.-214-5626_-214-5625insCCGGG
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