Canonical Allele Identifier: CA374264846

Gene: ALDOB

Linked Data

• dbSNP Id: rs766027880
• gnomAD v2: 9-104187855-T-C
• gnomAD v3: 9-101425573-T-C
• gnomAD v4: 9-101425573-T-C
• MyVariant Identifiers: chr9:g.104187855T>C (hg19) ; chr9:g.101425573T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425573T>C , CM000671.2:g.101425573T>C	GRCh38
NC_000009.11:g.104187855T>C , CM000671.1:g.104187855T>C	GRCh37
NC_000009.10:g.103227676T>C	NCBI36
NG_012387.1:g.15208A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.679A>G MANE Select	ENSP00000497767.1:p.Thr227Ala
ENST00000648064.1:c.679A>G	ENSP00000497990.1:p.Thr227Ala
ENST00000648758.1:c.679A>G	ENSP00000497731.1:p.Thr227Ala
ENST00000649902.1:c.679A>G	ENSP00000497216.1:p.Thr227Ala
ENST00000374855.8:c.679A>G	ENSP00000363988.4:p.Thr227Ala
ENST00000468981.3:n.206A>G
ENST00000616752.1:c.679A>G	ENSP00000481363.1:p.Thr227Ala
NM_000035.3:c.679A>G	NP_000026.2:p.Thr227Ala
NM_000035.4:c.679A>G MANE Select	NP_000026.2:p.Thr227Ala