Canonical Allele Identifier: CA196955845
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1012065747
gnomAD v2: 9-104184194-A-T
gnomAD v3: 9-101421912-A-T
gnomAD v4: 9-101421912-A-T
MyVariant Identifiers: chr9:g.104184194A>T (hg19) chr9:g.101421912A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421912A>T , CM000671.2:g.101421912A>T GRCh38
NC_000009.11:g.104184194A>T , CM000671.1:g.104184194A>T GRCh37
NC_000009.10:g.103224015A>T NCBI36
NG_012387.1:g.18869T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1000-8T>A MANE Select ENSP00000497767.1:n.1000-8T>A
ENST00000648064.1:c.1000-8T>A ENSP00000497990.1:n.1000-8T>A
ENST00000648758.1:c.1000-8T>A ENSP00000497731.1:n.1000-8T>A
ENST00000374855.8:c.1000-8T>A ENSP00000363988.4:n.1000-8T>A
ENST00000616752.1:c.*12-8T>A ENSP00000481363.1:n.*12-8T>A
NM_000035.3:c.1000-8T>A NP_000026.2:n.1000-8T>A
NM_000035.4:c.1000-8T>A MANE Select NP_000026.2:n.1000-8T>A
Search 100 bp 5'
Search 100 bp 3'