Canonical Allele Identifier: CA1868275527
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421783G= , CM000671.2:g.101421783G= GRCh38
NC_000009.11:g.104184065G= , CM000671.1:g.104184065G= GRCh37
NC_000009.10:g.103223886G= NCBI36
NG_012387.1:g.18998C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*26C= MANE Select ENSP00000497767.1:n.*26C=
ENST00000648064.1:c.*26C= ENSP00000497990.1:n.*26C=
ENST00000648758.1:c.*26C= ENSP00000497731.1:n.*26C=
ENST00000374855.8:c.*26C= ENSP00000363988.4:n.*26C=
ENST00000616752.1:c.*133C= ENSP00000481363.1:n.*133C=
NM_000035.3:c.*26C= NP_000026.2:n.*26C=
NM_000035.4:c.*26C= MANE Select NP_000026.2:n.*26C=