Canonical Allele Identifier: CA1868275142
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421386T= , CM000671.2:g.101421386T= GRCh38
NC_000009.11:g.104183668T= , CM000671.1:g.104183668T= GRCh37
NC_000009.10:g.103223489T= NCBI36
NG_012387.1:g.19395A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*423A= MANE Select ENSP00000497767.1:n.*423A=
ENST00000374855.8:c.*423A= ENSP00000363988.4:n.*423A=
NM_000035.3:c.*423A= NP_000026.2:n.*423A=
NM_000035.4:c.*423A= MANE Select NP_000026.2:n.*423A=