Canonical Allele Identifier: CA374265755

Gene: ALDOB

Linked Data

• dbSNP Id: rs1831190094
• gnomAD v3: 9-101429816-T-C
• gnomAD v4: 9-101429816-T-C
• MyVariant Identifiers: chr9:g.104192098T>C (hg19) ; chr9:g.101429816T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429816T>C , CM000671.2:g.101429816T>C	GRCh38
NC_000009.11:g.104192098T>C , CM000671.1:g.104192098T>C	GRCh37
NC_000009.10:g.103231919T>C	NCBI36
NG_012387.1:g.10965A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.263A>G MANE Select	ENSP00000497767.1:p.Asp88Gly
ENST00000648064.1:c.263A>G	ENSP00000497990.1:p.Asp88Gly
ENST00000648758.1:c.263A>G	ENSP00000497731.1:p.Asp88Gly
ENST00000648906.1:n.433A>G
ENST00000649902.1:c.263A>G	ENSP00000497216.1:p.Asp88Gly
ENST00000650613.1:n.339A>G
ENST00000374855.8:c.263A>G	ENSP00000363988.4:p.Asp88Gly
ENST00000468981.3:n.60A>G
ENST00000616752.1:c.263A>G	ENSP00000481363.1:p.Asp88Gly
NM_000035.3:c.263A>G	NP_000026.2:p.Asp88Gly
NM_000035.4:c.263A>G MANE Select	NP_000026.2:p.Asp88Gly