Canonical Allele Identifier: CA903828666

Gene: EHHADH

Linked Data

• dbSNP Id: rs1271356012
• MyVariant Identifiers: chr3:g.184972043_184972044insA (hg19) ; chr3:g.185254255_185254256insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185254256dup , CM000665.2:g.185254256dup	GRCh38
NC_000003.11:g.184972044dup , CM000665.1:g.184972044dup	GRCh37
NC_000003.10:g.186454738dup	NCBI36
NG_015999.1:g.4843dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465178.1:n.228-5739dup
XM_011512517.1:c.-214-5739dup	XP_011510819.1:n.-214-5739dup