Canonical Allele Identifier: CA2691007318
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101426671-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101426671G>A , CM000671.2:g.101426671G>A GRCh38
NC_000009.11:g.104188953G>A , CM000671.1:g.104188953G>A GRCh37
NC_000009.10:g.103228774G>A NCBI36
NG_012387.1:g.14110C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.541-33C>T MANE Select ENSP00000497767.1:n.541-33C>T
ENST00000648064.1:c.541-33C>T ENSP00000497990.1:n.541-33C>T
ENST00000648758.1:c.541-33C>T ENSP00000497731.1:n.541-33C>T
ENST00000649902.1:c.541-33C>T ENSP00000497216.1:n.541-33C>T
ENST00000374855.8:c.541-33C>T ENSP00000363988.4:n.541-33C>T
ENST00000468981.3:n.68-33C>T
ENST00000616752.1:c.541-33C>T ENSP00000481363.1:n.541-33C>T
NM_000035.3:c.541-33C>T NP_000026.2:n.541-33C>T
NM_000035.4:c.541-33C>T MANE Select NP_000026.2:n.541-33C>T
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