Canonical Allele Identifier: CA374265049
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1242518351

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101426588A>T , CM000671.2:g.101426588A>T GRCh38
NC_000009.11:g.104188870A>T , CM000671.1:g.104188870A>T GRCh37
NC_000009.10:g.103228691A>T NCBI36
NG_012387.1:g.14193T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.591T>A MANE Select ENSP00000497767.1:p.His197Gln
ENST00000648064.1:c.591T>A ENSP00000497990.1:p.His197Gln
ENST00000648758.1:c.591T>A ENSP00000497731.1:p.His197Gln
ENST00000649902.1:c.591T>A ENSP00000497216.1:p.His197Gln
ENST00000374855.8:c.591T>A ENSP00000363988.4:p.His197Gln
ENST00000468981.3:n.118T>A
ENST00000616752.1:c.591T>A ENSP00000481363.1:p.His197Gln
NM_000035.3:c.591T>A NP_000026.2:p.His197Gln
NM_000035.4:c.591T>A MANE Select NP_000026.2:p.His197Gln