Canonical Allele Identifier: CA857728294
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1342580025
MyVariant Identifiers: chr9:g.104183684T>A (hg19) chr9:g.101421402T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421402T>A , CM000671.2:g.101421402T>A GRCh38
NC_000009.11:g.104183684T>A , CM000671.1:g.104183684T>A GRCh37
NC_000009.10:g.103223505T>A NCBI36
NG_012387.1:g.19379A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*407A>T MANE Select ENSP00000497767.1:n.*407A>T
ENST00000374855.8:c.*407A>T ENSP00000363988.4:n.*407A>T
NM_000035.3:c.*407A>T NP_000026.2:n.*407A>T
NM_000035.4:c.*407A>T MANE Select NP_000026.2:n.*407A>T
Search 100 bp 5'
Search 100 bp 3'