Canonical Allele Identifier: CA374264771
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1831115180

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425534A>G , CM000671.2:g.101425534A>G GRCh38
NC_000009.11:g.104187816A>G , CM000671.1:g.104187816A>G GRCh37
NC_000009.10:g.103227637A>G NCBI36
NG_012387.1:g.15247T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.718T>C MANE Select ENSP00000497767.1:p.Cys240Arg
ENST00000648064.1:c.718T>C ENSP00000497990.1:p.Cys240Arg
ENST00000648758.1:c.718T>C ENSP00000497731.1:p.Cys240Arg
ENST00000649902.1:c.718T>C ENSP00000497216.1:p.Cys240Arg
ENST00000374855.8:c.718T>C ENSP00000363988.4:p.Cys240Arg
ENST00000616752.1:c.718T>C ENSP00000481363.1:p.Cys240Arg
NM_000035.3:c.718T>C NP_000026.2:p.Cys240Arg
NM_000035.4:c.718T>C MANE Select NP_000026.2:p.Cys240Arg