Canonical Allele Identifier: CA374265875
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429871T>C , CM000671.2:g.101429871T>C GRCh38
NC_000009.11:g.104192153T>C , CM000671.1:g.104192153T>C GRCh37
NC_000009.10:g.103231974T>C NCBI36
NG_012387.1:g.10910A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.208A>G MANE Select ENSP00000497767.1:p.Ile70Val
ENST00000648064.1:c.208A>G ENSP00000497990.1:p.Ile70Val
ENST00000648423.1:c.208A>G ENSP00000497985.1:p.Ile70Val
ENST00000648758.1:c.208A>G ENSP00000497731.1:p.Ile70Val
ENST00000648906.1:n.378A>G
ENST00000649902.1:c.208A>G ENSP00000497216.1:p.Ile70Val
ENST00000650613.1:n.284A>G
ENST00000374855.8:c.208A>G ENSP00000363988.4:p.Ile70Val
ENST00000468981.3:n.5A>G
ENST00000616752.1:c.208A>G ENSP00000481363.1:p.Ile70Val
NM_000035.3:c.208A>G NP_000026.2:p.Ile70Val
NM_000035.4:c.208A>G MANE Select NP_000026.2:p.Ile70Val