Canonical Allele Identifier: CA1868278366
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101424818T= , CM000671.2:g.101424818T= GRCh38
NC_000009.11:g.104187100T= , CM000671.1:g.104187100T= GRCh37
NC_000009.10:g.103226921T= NCBI36
NG_012387.1:g.15963A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.999+25A= MANE Select ENSP00000497767.1:n.999+25A=
ENST00000648064.1:c.999+25A= ENSP00000497990.1:n.999+25A=
ENST00000648758.1:c.999+25A= ENSP00000497731.1:n.999+25A=
ENST00000649902.1:c.1024A= ENSP00000497216.1:p.Thr342=
ENST00000374855.8:c.999+25A= ENSP00000363988.4:n.999+25A=
ENST00000616752.1:c.*11+25A= ENSP00000481363.1:n.*11+25A=
NM_000035.3:c.999+25A= NP_000026.2:n.999+25A=
NM_000035.4:c.999+25A= MANE Select NP_000026.2:n.999+25A=
Search 100 bp 5'
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