Canonical Allele Identifier: CA2785321718
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421432T>C , CM000671.2:g.101421432T>C GRCh38
NC_000009.11:g.104183714T>C , CM000671.1:g.104183714T>C GRCh37
NC_000009.10:g.103223535T>C NCBI36
NG_012387.1:g.19349A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*377A>G MANE Select ENSP00000497767.1:n.*377A>G
ENST00000374855.8:c.*377A>G ENSP00000363988.4:n.*377A>G
NM_000035.3:c.*377A>G NP_000026.2:n.*377A>G
NM_000035.4:c.*377A>G MANE Select NP_000026.2:n.*377A>G
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