Canonical Allele Identifier: CA374264618
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425456G>T , CM000671.2:g.101425456G>T GRCh38
NC_000009.11:g.104187738G>T , CM000671.1:g.104187738G>T GRCh37
NC_000009.10:g.103227559G>T NCBI36
NG_012387.1:g.15325C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.796C>A MANE Select ENSP00000497767.1:p.Pro266Thr
ENST00000648064.1:c.796C>A ENSP00000497990.1:p.Pro266Thr
ENST00000648758.1:c.796C>A ENSP00000497731.1:p.Pro266Thr
ENST00000649902.1:c.796C>A ENSP00000497216.1:p.Pro266Thr
ENST00000374855.8:c.796C>A ENSP00000363988.4:p.Pro266Thr
ENST00000616752.1:c.796C>A ENSP00000481363.1:p.Pro266Thr
NM_000035.3:c.796C>A NP_000026.2:p.Pro266Thr
NM_000035.4:c.796C>A MANE Select NP_000026.2:p.Pro266Thr