Canonical Allele Identifier: CA2739364

Gene: EHHADH

Linked Data

• dbSNP Id: rs779243157
• ExAC: 3:184971787 G / A
• gnomAD v2: 3-184971787-G-A
• gnomAD v4: 3-185253999-G-A
• MyVariant Identifiers: chr3:g.184971787G>A (hg19) ; chr3:g.185253999G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185253999G>A , CM000665.2:g.185253999G>A	GRCh38
NC_000003.11:g.184971787G>A , CM000665.1:g.184971787G>A	GRCh37
NC_000003.10:g.186454481G>A	NCBI36
NG_015999.1:g.5100C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231887.8:c.24C>T MANE Select	ENSP00000231887.3:p.His8=
ENST00000231887.7:c.24C>T	ENSP00000231887.3:p.His8=
ENST00000440662.1:c.24C>T	ENSP00000396798.1:p.His8=
ENST00000456310.5:c.-388C>T	ENSP00000387746.1:n.-388C>T
ENST00000465178.1:n.228-5482C>T
ENST00000475987.1:n.51C>T
NM_001166415.1:c.-388C>T	NP_001159887.1:n.-388C>T
NM_001966.3:c.24C>T	NP_001957.2:p.His8=
XM_006713525.1:c.-632C>T	XP_006713588.1:n.-632C>T
XM_011512517.1:c.-214-5482C>T	XP_011510819.1:n.-214-5482C>T
NM_001966.4:c.24C>T MANE Select	NP_001957.2:p.His8=
NM_001166415.2:c.-388C>T	NP_001159887.1:n.-388C>T