Canonical Allele Identifier: CA5161438
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 796044
ClinVar RCV Id: RCV000979403
dbSNP Id: rs765247994
ExAC: 9:104187251 A / T
gnomAD v2: 9-104187251-A-T
gnomAD v3: 9-101424969-A-T
gnomAD v4: 9-101424969-A-T
MyVariant Identifiers: chr9:g.104187251A>T (hg19) chr9:g.101424969A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101424969A>T , CM000671.2:g.101424969A>T GRCh38
NC_000009.11:g.104187251A>T , CM000671.1:g.104187251A>T GRCh37
NC_000009.10:g.103227072A>T NCBI36
NG_012387.1:g.15812T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.873T>A MANE Select ENSP00000497767.1:p.Pro291=
ENST00000648064.1:c.873T>A ENSP00000497990.1:p.Pro291=
ENST00000648758.1:c.873T>A ENSP00000497731.1:p.Pro291=
ENST00000649902.1:c.873T>A ENSP00000497216.1:p.Pro291=
ENST00000374855.8:c.873T>A ENSP00000363988.4:p.Pro291=
ENST00000616752.1:c.873T>A ENSP00000481363.1:p.Pro291=
NM_000035.3:c.873T>A NP_000026.2:p.Pro291=
NM_000035.4:c.873T>A MANE Select NP_000026.2:p.Pro291=
Search 100 bp 5'
Search 100 bp 3'