Canonical Allele Identifier: CA10628632
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 364305
ClinVar RCV Id: RCV000395004 RCV001683440
dbSNP Id: rs41310087
gnomAD v2: 9-104183969-C-T
gnomAD v3: 9-101421687-C-T
gnomAD v4: 9-101421687-C-T
MyVariant Identifiers: chr9:g.104183969C>T (hg19) chr9:g.101421687C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421687C>T , CM000671.2:g.101421687C>T GRCh38
NC_000009.11:g.104183969C>T , CM000671.1:g.104183969C>T GRCh37
NC_000009.10:g.103223790C>T NCBI36
NG_012387.1:g.19094G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*122G>A MANE Select ENSP00000497767.1:n.*122G>A
ENST00000648064.1:c.*122G>A ENSP00000497990.1:n.*122G>A
ENST00000648758.1:c.*122G>A ENSP00000497731.1:n.*122G>A
ENST00000374855.8:c.*122G>A ENSP00000363988.4:n.*122G>A
ENST00000616752.1:c.*229G>A ENSP00000481363.1:n.*229G>A
NM_000035.3:c.*122G>A NP_000026.2:n.*122G>A
NM_000035.4:c.*122G>A MANE Select NP_000026.2:n.*122G>A
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