Canonical Allele Identifier: CA374265332
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101427568G>C , CM000671.2:g.101427568G>C GRCh38
NC_000009.11:g.104189850G>C , CM000671.1:g.104189850G>C GRCh37
NC_000009.10:g.103229671G>C NCBI36
NG_012387.1:g.13213C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.454C>G MANE Select ENSP00000497767.1:p.Leu152Val
ENST00000648064.1:c.454C>G ENSP00000497990.1:p.Leu152Val
ENST00000648758.1:c.454C>G ENSP00000497731.1:p.Leu152Val
ENST00000649902.1:c.454C>G ENSP00000497216.1:p.Leu152Val
ENST00000374855.8:c.454C>G ENSP00000363988.4:p.Leu152Val
ENST00000468981.3:n.68-930C>G
ENST00000616752.1:c.454C>G ENSP00000481363.1:p.Leu152Val
NM_000035.3:c.454C>G NP_000026.2:p.Leu152Val
NM_000035.4:c.454C>G MANE Select NP_000026.2:p.Leu152Val