Canonical Allele Identifier: CA2691005952
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101429665-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429665G>T , CM000671.2:g.101429665G>T GRCh38
NC_000009.11:g.104191947G>T , CM000671.1:g.104191947G>T GRCh37
NC_000009.10:g.103231768G>T NCBI36
NG_012387.1:g.11116C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.324+90C>A MANE Select ENSP00000497767.1:n.324+90C>A
ENST00000648064.1:c.324+90C>A ENSP00000497990.1:n.324+90C>A
ENST00000648758.1:c.324+90C>A ENSP00000497731.1:n.324+90C>A
ENST00000648906.1:n.584C>A
ENST00000649902.1:c.324+90C>A ENSP00000497216.1:n.324+90C>A
ENST00000650613.1:n.490C>A
ENST00000374855.8:c.324+90C>A ENSP00000363988.4:n.324+90C>A
ENST00000468981.3:n.67+144C>A
ENST00000616752.1:c.324+90C>A ENSP00000481363.1:n.324+90C>A
NM_000035.3:c.324+90C>A NP_000026.2:n.324+90C>A
NM_000035.4:c.324+90C>A MANE Select NP_000026.2:n.324+90C>A
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