Canonical Allele Identifier: CA857728355
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1229347420
gnomAD v3: 9-101421472-A-T
gnomAD v4: 9-101421472-A-T
MyVariant Identifiers: chr9:g.104183754A>T (hg19) chr9:g.101421472A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421472A>T , CM000671.2:g.101421472A>T GRCh38
NC_000009.11:g.104183754A>T , CM000671.1:g.104183754A>T GRCh37
NC_000009.10:g.103223575A>T NCBI36
NG_012387.1:g.19309T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*337T>A MANE Select ENSP00000497767.1:n.*337T>A
ENST00000648064.1:c.*337T>A ENSP00000497990.1:n.*337T>A
ENST00000374855.8:c.*337T>A ENSP00000363988.4:n.*337T>A
NM_000035.3:c.*337T>A NP_000026.2:n.*337T>A
NM_000035.4:c.*337T>A MANE Select NP_000026.2:n.*337T>A
Search 100 bp 5'
Search 100 bp 3'