Canonical Allele Identifier: CA2785321766
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421796C>G , CM000671.2:g.101421796C>G GRCh38
NC_000009.11:g.104184078C>G , CM000671.1:g.104184078C>G GRCh37
NC_000009.10:g.103223899C>G NCBI36
NG_012387.1:g.18985G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*13G>C MANE Select ENSP00000497767.1:n.*13G>C
ENST00000648064.1:c.*13G>C ENSP00000497990.1:n.*13G>C
ENST00000648758.1:c.*13G>C ENSP00000497731.1:n.*13G>C
ENST00000374855.8:c.*13G>C ENSP00000363988.4:n.*13G>C
ENST00000616752.1:c.*120G>C ENSP00000481363.1:n.*120G>C
NM_000035.3:c.*13G>C NP_000026.2:n.*13G>C
NM_000035.4:c.*13G>C MANE Select NP_000026.2:n.*13G>C