Canonical Allele Identifier: CA1868279010
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425455G= , CM000671.2:g.101425455G= GRCh38
NC_000009.11:g.104187737G= , CM000671.1:g.104187737G= GRCh37
NC_000009.10:g.103227558G= NCBI36
NG_012387.1:g.15326C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.797C= MANE Select ENSP00000497767.1:p.Pro266=
ENST00000648064.1:c.797C= ENSP00000497990.1:p.Pro266=
ENST00000648758.1:c.797C= ENSP00000497731.1:p.Pro266=
ENST00000649902.1:c.797C= ENSP00000497216.1:p.Pro266=
ENST00000374855.8:c.797C= ENSP00000363988.4:p.Pro266=
ENST00000616752.1:c.797C= ENSP00000481363.1:p.Pro266=
NM_000035.3:c.797C= NP_000026.2:p.Pro266=
NM_000035.4:c.797C= MANE Select NP_000026.2:p.Pro266=