Canonical Allele Identifier: CA857730285
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1323081878
gnomAD v3: 9-101424659-G-T
gnomAD v4: 9-101424659-G-T
MyVariant Identifiers: chr9:g.104186941G>T (hg19) chr9:g.101424659G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101424659G>T , CM000671.2:g.101424659G>T GRCh38
NC_000009.11:g.104186941G>T , CM000671.1:g.104186941G>T GRCh37
NC_000009.10:g.103226762G>T NCBI36
NG_012387.1:g.16122C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.999+184C>A MANE Select ENSP00000497767.1:n.999+184C>A
ENST00000648064.1:c.999+184C>A ENSP00000497990.1:n.999+184C>A
ENST00000648758.1:c.999+184C>A ENSP00000497731.1:n.999+184C>A
ENST00000649902.1:c.*154C>A ENSP00000497216.1:n.*154C>A
ENST00000374855.8:c.999+184C>A ENSP00000363988.4:n.999+184C>A
ENST00000616752.1:c.*11+184C>A ENSP00000481363.1:n.*11+184C>A
NM_000035.3:c.999+184C>A NP_000026.2:n.999+184C>A
NM_000035.4:c.999+184C>A MANE Select NP_000026.2:n.999+184C>A
Search 100 bp 5'
Search 100 bp 3'