Canonical Allele Identifier: CA2691006257
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101421557-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421557G>T , CM000671.2:g.101421557G>T GRCh38
NC_000009.11:g.104183839G>T , CM000671.1:g.104183839G>T GRCh37
NC_000009.10:g.103223660G>T NCBI36
NG_012387.1:g.19224C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*252C>A MANE Select ENSP00000497767.1:n.*252C>A
ENST00000648064.1:c.*252C>A ENSP00000497990.1:n.*252C>A
ENST00000374855.8:c.*252C>A ENSP00000363988.4:n.*252C>A
ENST00000616752.1:c.*359C>A ENSP00000481363.1:n.*359C>A
NM_000035.3:c.*252C>A NP_000026.2:n.*252C>A
NM_000035.4:c.*252C>A MANE Select NP_000026.2:n.*252C>A
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