Canonical Allele Identifier: CA10631890
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 364296
ClinVar RCV Id: RCV000358465
dbSNP Id: rs41296049
gnomAD v2: 9-104183479-T-C
gnomAD v3: 9-101421197-T-C
gnomAD v4: 9-101421197-T-C
MyVariant Identifiers: chr9:g.104183479T>C (hg19) chr9:g.101421197T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421197T>C , CM000671.2:g.101421197T>C GRCh38
NC_000009.11:g.104183479T>C , CM000671.1:g.104183479T>C GRCh37
NC_000009.10:g.103223300T>C NCBI36
NG_012387.1:g.19584A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*612A>G MANE Select ENSP00000497767.1:n.*612A>G
ENST00000374855.8:c.*612A>G ENSP00000363988.4:n.*612A>G
NM_000035.3:c.*612A>G NP_000026.2:n.*612A>G
NM_000035.4:c.*612A>G MANE Select NP_000026.2:n.*612A>G
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Search 100 bp 3'