Canonical Allele Identifier: CA196956551

Gene: ALDOB

Linked Data

• dbSNP Id: rs148100257
• gnomAD v3: 9-101424771-G-T
• gnomAD v4: 9-101424771-G-T
• MyVariant Identifiers: chr9:g.104187053G>T (hg19) ; chr9:g.101424771G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424771G>T , CM000671.2:g.101424771G>T	GRCh38
NC_000009.11:g.104187053G>T , CM000671.1:g.104187053G>T	GRCh37
NC_000009.10:g.103226874G>T	NCBI36
NG_012387.1:g.16010C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.999+72C>A MANE Select	ENSP00000497767.1:n.999+72C>A
ENST00000648064.1:c.999+72C>A	ENSP00000497990.1:n.999+72C>A
ENST00000648758.1:c.999+72C>A	ENSP00000497731.1:n.999+72C>A
ENST00000649902.1:c.*42C>A	ENSP00000497216.1:n.*42C>A
ENST00000374855.8:c.999+72C>A	ENSP00000363988.4:n.999+72C>A
ENST00000616752.1:c.*11+72C>A	ENSP00000481363.1:n.*11+72C>A
NM_000035.3:c.999+72C>A	NP_000026.2:n.999+72C>A
NM_000035.4:c.999+72C>A MANE Select	NP_000026.2:n.999+72C>A