Canonical Allele Identifier: CA2668886408
Gene: EHHADH HGNC NCBI

Linked Data

gnomAD v4: 3-185254214-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254214G>T , CM000665.2:g.185254214G>T GRCh38
NC_000003.11:g.184972002G>T , CM000665.1:g.184972002G>T GRCh37
NC_000003.10:g.186454696G>T NCBI36
NG_015999.1:g.4885C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5697C>A
XM_011512517.1:c.-214-5697C>A XP_011510819.1:n.-214-5697C>A
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