Canonical Allele Identifier: CA196956541

Gene: ALDOB

Linked Data

• dbSNP Id: rs891703200
• gnomAD v4: 9-101424763-A-G
• MyVariant Identifiers: chr9:g.104187045A>G (hg19) ; chr9:g.101424763A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424763A>G , CM000671.2:g.101424763A>G	GRCh38
NC_000009.11:g.104187045A>G , CM000671.1:g.104187045A>G	GRCh37
NC_000009.10:g.103226866A>G	NCBI36
NG_012387.1:g.16018T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.999+80T>C MANE Select	ENSP00000497767.1:n.999+80T>C
ENST00000648064.1:c.999+80T>C	ENSP00000497990.1:n.999+80T>C
ENST00000648758.1:c.999+80T>C	ENSP00000497731.1:n.999+80T>C
ENST00000649902.1:c.*50T>C	ENSP00000497216.1:n.*50T>C
ENST00000374855.8:c.999+80T>C	ENSP00000363988.4:n.999+80T>C
ENST00000616752.1:c.*11+80T>C	ENSP00000481363.1:n.*11+80T>C
NM_000035.3:c.999+80T>C	NP_000026.2:n.999+80T>C
NM_000035.4:c.999+80T>C MANE Select	NP_000026.2:n.999+80T>C