Canonical Allele Identifier: CA10631891
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 364302
ClinVar RCV Id: RCV000375109
dbSNP Id: rs142431256
gnomAD v2: 9-104183823-A-G
gnomAD v3: 9-101421541-A-G
gnomAD v4: 9-101421541-A-G
MyVariant Identifiers: chr9:g.104183823A>G (hg19) chr9:g.101421541A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421541A>G , CM000671.2:g.101421541A>G GRCh38
NC_000009.11:g.104183823A>G , CM000671.1:g.104183823A>G GRCh37
NC_000009.10:g.103223644A>G NCBI36
NG_012387.1:g.19240T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*268T>C MANE Select ENSP00000497767.1:n.*268T>C
ENST00000648064.1:c.*268T>C ENSP00000497990.1:n.*268T>C
ENST00000374855.8:c.*268T>C ENSP00000363988.4:n.*268T>C
NM_000035.3:c.*268T>C NP_000026.2:n.*268T>C
NM_000035.4:c.*268T>C MANE Select NP_000026.2:n.*268T>C
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