Canonical Allele Identifier: CA2531134749
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421705C>T , CM000671.2:g.101421705C>T GRCh38
NC_000009.11:g.104183987C>T , CM000671.1:g.104183987C>T GRCh37
NC_000009.10:g.103223808C>T NCBI36
NG_012387.1:g.19076G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*104G>A MANE Select ENSP00000497767.1:n.*104G>A
ENST00000648064.1:c.*104G>A ENSP00000497990.1:n.*104G>A
ENST00000648758.1:c.*104G>A ENSP00000497731.1:n.*104G>A
ENST00000374855.8:c.*104G>A ENSP00000363988.4:n.*104G>A
ENST00000616752.1:c.*211G>A ENSP00000481363.1:n.*211G>A
NM_000035.3:c.*104G>A NP_000026.2:n.*104G>A
NM_000035.4:c.*104G>A MANE Select NP_000026.2:n.*104G>A