Canonical Allele Identifier: CA196955729
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs958144429

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421672G>A , CM000671.2:g.101421672G>A GRCh38
NC_000009.11:g.104183954G>A , CM000671.1:g.104183954G>A GRCh37
NC_000009.10:g.103223775G>A NCBI36
NG_012387.1:g.19109C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*137C>T MANE Select ENSP00000497767.1:n.*137C>T
ENST00000648064.1:c.*137C>T ENSP00000497990.1:n.*137C>T
ENST00000648758.1:c.*137C>T ENSP00000497731.1:n.*137C>T
ENST00000374855.8:c.*137C>T ENSP00000363988.4:n.*137C>T
ENST00000616752.1:c.*244C>T ENSP00000481363.1:n.*244C>T
NM_000035.3:c.*137C>T NP_000026.2:n.*137C>T
NM_000035.4:c.*137C>T MANE Select NP_000026.2:n.*137C>T