Canonical Allele Identifier: CA5161499
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 364309
ClinVar RCV Id: RCV000401870
dbSNP Id: rs777324536

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425554A>T , CM000671.2:g.101425554A>T GRCh38
NC_000009.11:g.104187836A>T , CM000671.1:g.104187836A>T GRCh37
NC_000009.10:g.103227657A>T NCBI36
NG_012387.1:g.15227T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.698T>A MANE Select ENSP00000497767.1:p.Met233Lys
ENST00000648064.1:c.698T>A ENSP00000497990.1:p.Met233Lys
ENST00000648758.1:c.698T>A ENSP00000497731.1:p.Met233Lys
ENST00000649902.1:c.698T>A ENSP00000497216.1:p.Met233Lys
ENST00000374855.8:c.698T>A ENSP00000363988.4:p.Met233Lys
ENST00000616752.1:c.698T>A ENSP00000481363.1:p.Met233Lys
NM_000035.3:c.698T>A NP_000026.2:p.Met233Lys
NM_000035.4:c.698T>A MANE Select NP_000026.2:p.Met233Lys