Canonical Allele Identifier: CA1868275186
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421435C= , CM000671.2:g.101421435C= GRCh38
NC_000009.11:g.104183717C= , CM000671.1:g.104183717C= GRCh37
NC_000009.10:g.103223538C= NCBI36
NG_012387.1:g.19346G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*374G= MANE Select ENSP00000497767.1:n.*374G=
ENST00000374855.8:c.*374G= ENSP00000363988.4:n.*374G=
NM_000035.3:c.*374G= NP_000026.2:n.*374G=
NM_000035.4:c.*374G= MANE Select NP_000026.2:n.*374G=