Canonical Allele Identifier: CA1868279002
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425447C= , CM000671.2:g.101425447C= GRCh38
NC_000009.11:g.104187729C= , CM000671.1:g.104187729C= GRCh37
NC_000009.10:g.103227550C= NCBI36
NG_012387.1:g.15334G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.799+6G= MANE Select ENSP00000497767.1:n.799+6G=
ENST00000648064.1:c.799+6G= ENSP00000497990.1:n.799+6G=
ENST00000648758.1:c.799+6G= ENSP00000497731.1:n.799+6G=
ENST00000649902.1:c.799+6G= ENSP00000497216.1:n.799+6G=
ENST00000374855.8:c.799+6G= ENSP00000363988.4:n.799+6G=
ENST00000616752.1:c.799+6G= ENSP00000481363.1:n.799+6G=
NM_000035.3:c.799+6G= NP_000026.2:n.799+6G=
NM_000035.4:c.799+6G= MANE Select NP_000026.2:n.799+6G=