Canonical Allele Identifier: CA2691006351
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101421704-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421704G>T , CM000671.2:g.101421704G>T GRCh38
NC_000009.11:g.104183986G>T , CM000671.1:g.104183986G>T GRCh37
NC_000009.10:g.103223807G>T NCBI36
NG_012387.1:g.19077C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*105C>A MANE Select ENSP00000497767.1:n.*105C>A
ENST00000648064.1:c.*105C>A ENSP00000497990.1:n.*105C>A
ENST00000648758.1:c.*105C>A ENSP00000497731.1:n.*105C>A
ENST00000374855.8:c.*105C>A ENSP00000363988.4:n.*105C>A
ENST00000616752.1:c.*212C>A ENSP00000481363.1:n.*212C>A
NM_000035.3:c.*105C>A NP_000026.2:n.*105C>A
NM_000035.4:c.*105C>A MANE Select NP_000026.2:n.*105C>A
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