Canonical Allele Identifier: CA466462875

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104189806T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101427524T>C , CM000671.2:g.101427524T>C	GRCh38
NC_000009.11:g.104189806T>C , CM000671.1:g.104189806T>C	GRCh37
NC_000009.10:g.103229627T>C	NCBI36
NG_012387.1:g.13257A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.498A>G MANE Select	ENSP00000497767.1:p.Glu166=
ENST00000648064.1:c.498A>G	ENSP00000497990.1:p.Glu166=
ENST00000648758.1:c.498A>G	ENSP00000497731.1:p.Glu166=
ENST00000649902.1:c.498A>G	ENSP00000497216.1:p.Glu166=
ENST00000374855.8:c.498A>G	ENSP00000363988.4:p.Glu166=
ENST00000468981.3:n.68-886A>G
ENST00000616752.1:c.498A>G	ENSP00000481363.1:p.Glu166=
NM_000035.3:c.498A>G	NP_000026.2:p.Glu166=
NM_000035.4:c.498A>G MANE Select	NP_000026.2:p.Glu166=