Canonical Allele Identifier: CA1868275161
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421403T= , CM000671.2:g.101421403T= GRCh38
NC_000009.11:g.104183685T= , CM000671.1:g.104183685T= GRCh37
NC_000009.10:g.103223506T= NCBI36
NG_012387.1:g.19378A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*406A= MANE Select ENSP00000497767.1:n.*406A=
ENST00000374855.8:c.*406A= ENSP00000363988.4:n.*406A=
NM_000035.3:c.*406A= NP_000026.2:n.*406A=
NM_000035.4:c.*406A= MANE Select NP_000026.2:n.*406A=