Canonical Allele Identifier: CA1868281218
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429976G= , CM000671.2:g.101429976G= GRCh38
NC_000009.11:g.104192258G= , CM000671.1:g.104192258G= GRCh37
NC_000009.10:g.103232079G= NCBI36
NG_012387.1:g.10805C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.113-10C= MANE Select ENSP00000497767.1:n.113-10C=
ENST00000648064.1:c.113-10C= ENSP00000497990.1:n.113-10C=
ENST00000648423.1:c.113-10C= ENSP00000497985.1:n.113-10C=
ENST00000648758.1:c.113-10C= ENSP00000497731.1:n.113-10C=
ENST00000648906.1:n.283-10C=
ENST00000649902.1:c.113-10C= ENSP00000497216.1:n.113-10C=
ENST00000650613.1:n.189-10C=
ENST00000374855.8:c.113-10C= ENSP00000363988.4:n.113-10C=
ENST00000616752.1:c.113-10C= ENSP00000481363.1:n.113-10C=
NM_000035.3:c.113-10C= NP_000026.2:n.113-10C=
NM_000035.4:c.113-10C= MANE Select NP_000026.2:n.113-10C=