Canonical Allele Identifier: CA2691006250
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101421550-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421550T>C , CM000671.2:g.101421550T>C GRCh38
NC_000009.11:g.104183832T>C , CM000671.1:g.104183832T>C GRCh37
NC_000009.10:g.103223653T>C NCBI36
NG_012387.1:g.19231A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*259A>G MANE Select ENSP00000497767.1:n.*259A>G
ENST00000648064.1:c.*259A>G ENSP00000497990.1:n.*259A>G
ENST00000374855.8:c.*259A>G ENSP00000363988.4:n.*259A>G
NM_000035.3:c.*259A>G NP_000026.2:n.*259A>G
NM_000035.4:c.*259A>G MANE Select NP_000026.2:n.*259A>G
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