Canonical Allele Identifier: CA2691006349
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101421702-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421702C>A , CM000671.2:g.101421702C>A GRCh38
NC_000009.11:g.104183984C>A , CM000671.1:g.104183984C>A GRCh37
NC_000009.10:g.103223805C>A NCBI36
NG_012387.1:g.19079G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*107G>T MANE Select ENSP00000497767.1:n.*107G>T
ENST00000648064.1:c.*107G>T ENSP00000497990.1:n.*107G>T
ENST00000648758.1:c.*107G>T ENSP00000497731.1:n.*107G>T
ENST00000374855.8:c.*107G>T ENSP00000363988.4:n.*107G>T
ENST00000616752.1:c.*214G>T ENSP00000481363.1:n.*214G>T
NM_000035.3:c.*107G>T NP_000026.2:n.*107G>T
NM_000035.4:c.*107G>T MANE Select NP_000026.2:n.*107G>T
Search 100 bp 5'
Search 100 bp 3'