Canonical Allele Identifier: CA466462951
Gene: ALDOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104190758G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101428476G>T , CM000671.2:g.101428476G>T GRCh38
NC_000009.11:g.104190758G>T , CM000671.1:g.104190758G>T GRCh37
NC_000009.10:g.103230579G>T NCBI36
NG_012387.1:g.12305C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.372C>A MANE Select ENSP00000497767.1:p.Thr124=
ENST00000648064.1:c.372C>A ENSP00000497990.1:p.Thr124=
ENST00000648758.1:c.372C>A ENSP00000497731.1:p.Thr124=
ENST00000649902.1:c.372C>A ENSP00000497216.1:p.Thr124=
ENST00000374855.8:c.372C>A ENSP00000363988.4:p.Thr124=
ENST00000468981.3:n.67+1333C>A
ENST00000616752.1:c.372C>A ENSP00000481363.1:p.Thr124=
NM_000035.3:c.372C>A NP_000026.2:p.Thr124=
NM_000035.4:c.372C>A MANE Select NP_000026.2:p.Thr124=
Search 100 bp 5'
Search 100 bp 3'