Canonical Allele Identifier: CA374264608
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1065878
ClinVar RCV Id: RCV001376732
dbSNP Id: rs2118345193

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425451A>T , CM000671.2:g.101425451A>T GRCh38
NC_000009.11:g.104187733A>T , CM000671.1:g.104187733A>T GRCh37
NC_000009.10:g.103227554A>T NCBI36
NG_012387.1:g.15330T>A

Transcript Alleles

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