Canonical Allele Identifier: CA2785321714
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421378A>T , CM000671.2:g.101421378A>T GRCh38
NC_000009.11:g.104183660A>T , CM000671.1:g.104183660A>T GRCh37
NC_000009.10:g.103223481A>T NCBI36
NG_012387.1:g.19403T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*431T>A MANE Select ENSP00000497767.1:n.*431T>A
ENST00000374855.8:c.*431T>A ENSP00000363988.4:n.*431T>A
NM_000035.3:c.*431T>A NP_000026.2:n.*431T>A
NM_000035.4:c.*431T>A MANE Select NP_000026.2:n.*431T>A