Canonical Allele Identifier: CA466463116

Gene: ALDOB

Linked Data

• ClinVar Variation Id: 1661063
• ClinVar RCV Id: RCV002190786
• dbSNP Id: rs928855259
• gnomAD v4: 9-101430792-A-C
• MyVariant Identifiers: chr9:g.104193074A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430792A>C , CM000671.2:g.101430792A>C	GRCh38
NC_000009.11:g.104193074A>C , CM000671.1:g.104193074A>C	GRCh37
NC_000009.10:g.103232895A>C	NCBI36
NG_012387.1:g.9989T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.96T>G MANE Select	ENSP00000497767.1:p.Ala32=
ENST00000648064.1:c.96T>G	ENSP00000497990.1:p.Ala32=
ENST00000648423.1:c.96T>G	ENSP00000497985.1:p.Ala32=
ENST00000648758.1:c.96T>G	ENSP00000497731.1:p.Ala32=
ENST00000648906.1:n.266T>G
ENST00000649902.1:c.96T>G	ENSP00000497216.1:p.Ala32=
ENST00000650613.1:n.172T>G
ENST00000374855.8:c.96T>G	ENSP00000363988.4:p.Ala32=
ENST00000616752.1:c.96T>G	ENSP00000481363.1:p.Ala32=
NM_000035.3:c.96T>G	NP_000026.2:p.Ala32=
NM_000035.4:c.96T>G MANE Select	NP_000026.2:p.Ala32=