Canonical Allele Identifier: CA1868275314
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421584G= , CM000671.2:g.101421584G= GRCh38
NC_000009.11:g.104183866G= , CM000671.1:g.104183866G= GRCh37
NC_000009.10:g.103223687G= NCBI36
NG_012387.1:g.19197C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*225C= MANE Select ENSP00000497767.1:n.*225C=
ENST00000648064.1:c.*225C= ENSP00000497990.1:n.*225C=
ENST00000374855.8:c.*225C= ENSP00000363988.4:n.*225C=
ENST00000616752.1:c.*332C= ENSP00000481363.1:n.*332C=
NM_000035.3:c.*225C= NP_000026.2:n.*225C=
NM_000035.4:c.*225C= MANE Select NP_000026.2:n.*225C=
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