Canonical Allele Identifier: CA466462019

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104187808C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425526C>T , CM000671.2:g.101425526C>T	GRCh38
NC_000009.11:g.104187808C>T , CM000671.1:g.104187808C>T	GRCh37
NC_000009.10:g.103227629C>T	NCBI36
NG_012387.1:g.15255G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.726G>A MANE Select	ENSP00000497767.1:p.Lys242=
ENST00000648064.1:c.726G>A	ENSP00000497990.1:p.Lys242=
ENST00000648758.1:c.726G>A	ENSP00000497731.1:p.Lys242=
ENST00000649902.1:c.726G>A	ENSP00000497216.1:p.Lys242=
ENST00000374855.8:c.726G>A	ENSP00000363988.4:p.Lys242=
ENST00000616752.1:c.726G>A	ENSP00000481363.1:p.Lys242=
NM_000035.3:c.726G>A	NP_000026.2:p.Lys242=
NM_000035.4:c.726G>A MANE Select	NP_000026.2:p.Lys242=