Canonical Allele Identifier: CA374264134
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1311241789

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421901T>A , CM000671.2:g.101421901T>A GRCh38
NC_000009.11:g.104184183T>A , CM000671.1:g.104184183T>A GRCh37
NC_000009.10:g.103224004T>A NCBI36
NG_012387.1:g.18880A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1003A>T MANE Select ENSP00000497767.1:p.Asn335Tyr
ENST00000648064.1:c.1003A>T ENSP00000497990.1:p.Asn335Tyr
ENST00000648758.1:c.1003A>T ENSP00000497731.1:p.Asn335Tyr
ENST00000374855.8:c.1003A>T ENSP00000363988.4:p.Asn335Tyr
ENST00000616752.1:c.*15A>T ENSP00000481363.1:n.*15A>T
NM_000035.3:c.1003A>T NP_000026.2:p.Asn335Tyr
NM_000035.4:c.1003A>T MANE Select NP_000026.2:p.Asn335Tyr