Canonical Allele Identifier: CA374264798
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425549T>C , CM000671.2:g.101425549T>C GRCh38
NC_000009.11:g.104187831T>C , CM000671.1:g.104187831T>C GRCh37
NC_000009.10:g.103227652T>C NCBI36
NG_012387.1:g.15232A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.703A>G MANE Select ENSP00000497767.1:p.Thr235Ala
ENST00000648064.1:c.703A>G ENSP00000497990.1:p.Thr235Ala
ENST00000648758.1:c.703A>G ENSP00000497731.1:p.Thr235Ala
ENST00000649902.1:c.703A>G ENSP00000497216.1:p.Thr235Ala
ENST00000374855.8:c.703A>G ENSP00000363988.4:p.Thr235Ala
ENST00000616752.1:c.703A>G ENSP00000481363.1:p.Thr235Ala
NM_000035.3:c.703A>G NP_000026.2:p.Thr235Ala
NM_000035.4:c.703A>G MANE Select NP_000026.2:p.Thr235Ala