Canonical Allele Identifier: CA1868278988
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425434A= , CM000671.2:g.101425434A= GRCh38
NC_000009.11:g.104187716A= , CM000671.1:g.104187716A= GRCh37
NC_000009.10:g.103227537A= NCBI36
NG_012387.1:g.15347T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.799+19T= MANE Select ENSP00000497767.1:n.799+19T=
ENST00000648064.1:c.799+19T= ENSP00000497990.1:n.799+19T=
ENST00000648758.1:c.799+19T= ENSP00000497731.1:n.799+19T=
ENST00000649902.1:c.799+19T= ENSP00000497216.1:n.799+19T=
ENST00000374855.8:c.799+19T= ENSP00000363988.4:n.799+19T=
ENST00000616752.1:c.799+19T= ENSP00000481363.1:n.799+19T=
NM_000035.3:c.799+19T= NP_000026.2:n.799+19T=
NM_000035.4:c.799+19T= MANE Select NP_000026.2:n.799+19T=