Canonical Allele Identifier: CA374264145
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421905C>T , CM000671.2:g.101421905C>T GRCh38
NC_000009.11:g.104184187C>T , CM000671.1:g.104184187C>T GRCh37
NC_000009.10:g.103224008C>T NCBI36
NG_012387.1:g.18876G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1000-1G>A MANE Select ENSP00000497767.1:n.1000-1G>A
ENST00000648064.1:c.1000-1G>A ENSP00000497990.1:n.1000-1G>A
ENST00000648758.1:c.1000-1G>A ENSP00000497731.1:n.1000-1G>A
ENST00000374855.8:c.1000-1G>A ENSP00000363988.4:n.1000-1G>A
ENST00000616752.1:c.*12-1G>A ENSP00000481363.1:n.*12-1G>A
NM_000035.3:c.1000-1G>A NP_000026.2:n.1000-1G>A
NM_000035.4:c.1000-1G>A MANE Select NP_000026.2:n.1000-1G>A