Canonical Allele Identifier: CA5161582
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs370367583

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101427519G>A , CM000671.2:g.101427519G>A GRCh38
NC_000009.11:g.104189801G>A , CM000671.1:g.104189801G>A GRCh37
NC_000009.10:g.103229622G>A NCBI36
NG_012387.1:g.13262C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.503C>T MANE Select ENSP00000497767.1:p.Ala168Val
ENST00000648064.1:c.503C>T ENSP00000497990.1:p.Ala168Val
ENST00000648758.1:c.503C>T ENSP00000497731.1:p.Ala168Val
ENST00000649902.1:c.503C>T ENSP00000497216.1:p.Ala168Val
ENST00000374855.8:c.503C>T ENSP00000363988.4:p.Ala168Val
ENST00000468981.3:n.68-881C>T
ENST00000616752.1:c.503C>T ENSP00000481363.1:p.Ala168Val
NM_000035.3:c.503C>T NP_000026.2:p.Ala168Val
NM_000035.4:c.503C>T MANE Select NP_000026.2:p.Ala168Val