Canonical Allele Identifier: CA1127395626
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1831044369
gnomAD v3: 9-101421414-G-C
gnomAD v4: 9-101421414-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421414G>C , CM000671.2:g.101421414G>C GRCh38
NC_000009.11:g.104183696G>C , CM000671.1:g.104183696G>C GRCh37
NC_000009.10:g.103223517G>C NCBI36
NG_012387.1:g.19367C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*395C>G MANE Select ENSP00000497767.1:n.*395C>G
ENST00000374855.8:c.*395C>G ENSP00000363988.4:n.*395C>G
NM_000035.3:c.*395C>G NP_000026.2:n.*395C>G
NM_000035.4:c.*395C>G MANE Select NP_000026.2:n.*395C>G
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