Canonical Allele Identifier: CA589815762

Gene: ALDOB

Linked Data

• dbSNP Id: rs1417821632
• gnomAD v2: 9-104192023-A-C
• gnomAD v4: 9-101429741-A-C
• MyVariant Identifiers: chr9:g.104192023A>C (hg19) ; chr9:g.101429741A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429741A>C , CM000671.2:g.101429741A>C	GRCh38
NC_000009.11:g.104192023A>C , CM000671.1:g.104192023A>C	GRCh37
NC_000009.10:g.103231844A>C	NCBI36
NG_012387.1:g.11040T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+14T>G MANE Select	ENSP00000497767.1:n.324+14T>G
ENST00000648064.1:c.324+14T>G	ENSP00000497990.1:n.324+14T>G
ENST00000648758.1:c.324+14T>G	ENSP00000497731.1:n.324+14T>G
ENST00000648906.1:n.508T>G
ENST00000649902.1:c.324+14T>G	ENSP00000497216.1:n.324+14T>G
ENST00000650613.1:n.414T>G
ENST00000374855.8:c.324+14T>G	ENSP00000363988.4:n.324+14T>G
ENST00000468981.3:n.67+68T>G
ENST00000616752.1:c.324+14T>G	ENSP00000481363.1:n.324+14T>G
NM_000035.3:c.324+14T>G	NP_000026.2:n.324+14T>G
NM_000035.4:c.324+14T>G MANE Select	NP_000026.2:n.324+14T>G