Canonical Allele Identifier: CA1868275166
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421414G= , CM000671.2:g.101421414G= GRCh38
NC_000009.11:g.104183696G= , CM000671.1:g.104183696G= GRCh37
NC_000009.10:g.103223517G= NCBI36
NG_012387.1:g.19367C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*395C= MANE Select ENSP00000497767.1:n.*395C=
ENST00000374855.8:c.*395C= ENSP00000363988.4:n.*395C=
NM_000035.3:c.*395C= NP_000026.2:n.*395C=
NM_000035.4:c.*395C= MANE Select NP_000026.2:n.*395C=