Canonical Allele Identifier: CA89521590
Gene: EHHADH HGNC NCBI

Linked Data

dbSNP Id: rs981538035
MyVariant Identifiers: chr3:g.184972135G>A (hg19) chr3:g.185254347G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185254347G>A , CM000665.2:g.185254347G>A GRCh38
NC_000003.11:g.184972135G>A , CM000665.1:g.184972135G>A GRCh37
NC_000003.10:g.186454829G>A NCBI36
NG_015999.1:g.4752C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465178.1:n.228-5830C>T
XM_011512517.1:c.-214-5830C>T XP_011510819.1:n.-214-5830C>T
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