Canonical Allele Identifier: CA2579403763
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101430691T>C , CM000671.2:g.101430691T>C GRCh38
NC_000009.11:g.104192973T>C , CM000671.1:g.104192973T>C GRCh37
NC_000009.10:g.103232794T>C NCBI36
NG_012387.1:g.10090A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.112+85A>G MANE Select ENSP00000497767.1:n.112+85A>G
ENST00000648064.1:c.112+85A>G ENSP00000497990.1:n.112+85A>G
ENST00000648423.1:c.112+85A>G ENSP00000497985.1:n.112+85A>G
ENST00000648758.1:c.112+85A>G ENSP00000497731.1:n.112+85A>G
ENST00000648906.1:n.282+85A>G
ENST00000649902.1:c.112+85A>G ENSP00000497216.1:n.112+85A>G
ENST00000650613.1:n.188+85A>G
ENST00000374855.8:c.112+85A>G ENSP00000363988.4:n.112+85A>G
ENST00000616752.1:c.112+85A>G ENSP00000481363.1:n.112+85A>G
NM_000035.3:c.112+85A>G NP_000026.2:n.112+85A>G
NM_000035.4:c.112+85A>G MANE Select NP_000026.2:n.112+85A>G