Canonical Allele Identifier: CA466463068

Gene: ALDOB

Linked Data

• dbSNP Id: rs1405787545
• gnomAD v2: 9-104192187-C-T
• gnomAD v4: 9-101429905-C-T
• MyVariant Identifiers: chr9:g.104192187C>T (hg19) ; chr9:g.101429905C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429905C>T , CM000671.2:g.101429905C>T	GRCh38
NC_000009.11:g.104192187C>T , CM000671.1:g.104192187C>T	GRCh37
NC_000009.10:g.103232008C>T	NCBI36
NG_012387.1:g.10876G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.174G>A MANE Select	ENSP00000497767.1:p.Gln58=
ENST00000648064.1:c.174G>A	ENSP00000497990.1:p.Gln58=
ENST00000648423.1:c.174G>A	ENSP00000497985.1:p.Gln58=
ENST00000648758.1:c.174G>A	ENSP00000497731.1:p.Gln58=
ENST00000648906.1:n.344G>A
ENST00000649902.1:c.174G>A	ENSP00000497216.1:p.Gln58=
ENST00000650613.1:n.250G>A
ENST00000374855.8:c.174G>A	ENSP00000363988.4:p.Gln58=
ENST00000616752.1:c.174G>A	ENSP00000481363.1:p.Gln58=
NM_000035.3:c.174G>A	NP_000026.2:p.Gln58=
NM_000035.4:c.174G>A MANE Select	NP_000026.2:p.Gln58=