Canonical Allele Identifier: CA653204408
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421373A>T , CM000671.2:g.101421373A>T GRCh38
NC_000009.11:g.104183655A>T , CM000671.1:g.104183655A>T GRCh37
NC_000009.10:g.103223476A>T NCBI36
NG_012387.1:g.19408T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*436T>A MANE Select ENSP00000497767.1:n.*436T>A
ENST00000374855.8:c.*436T>A ENSP00000363988.4:n.*436T>A
NM_000035.3:c.*436T>A NP_000026.2:n.*436T>A
NM_000035.4:c.*436T>A MANE Select NP_000026.2:n.*436T>A