Canonical Allele Identifier: CA590045553
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2916289
ClinVar RCV Id: RCV003598786
dbSNP Id: rs1361016269

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429983A>G , CM000671.2:g.101429983A>G GRCh38
NC_000009.11:g.104192265A>G , CM000671.1:g.104192265A>G GRCh37
NC_000009.10:g.103232086A>G NCBI36
NG_012387.1:g.10798T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.113-17T>C MANE Select ENSP00000497767.1:n.113-17T>C
ENST00000648064.1:c.113-17T>C ENSP00000497990.1:n.113-17T>C
ENST00000648423.1:c.113-17T>C ENSP00000497985.1:n.113-17T>C
ENST00000648758.1:c.113-17T>C ENSP00000497731.1:n.113-17T>C
ENST00000648906.1:n.283-17T>C
ENST00000649902.1:c.113-17T>C ENSP00000497216.1:n.113-17T>C
ENST00000650613.1:n.189-17T>C
ENST00000374855.8:c.113-17T>C ENSP00000363988.4:n.113-17T>C
ENST00000616752.1:c.113-17T>C ENSP00000481363.1:n.113-17T>C
NM_000035.3:c.113-17T>C NP_000026.2:n.113-17T>C
NM_000035.4:c.113-17T>C MANE Select NP_000026.2:n.113-17T>C