Canonical Allele Identifier: CA1868279013
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425457A= , CM000671.2:g.101425457A= GRCh38
NC_000009.11:g.104187739A= , CM000671.1:g.104187739A= GRCh37
NC_000009.10:g.103227560A= NCBI36
NG_012387.1:g.15324T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.795T= MANE Select ENSP00000497767.1:p.Val265=
ENST00000648064.1:c.795T= ENSP00000497990.1:p.Val265=
ENST00000648758.1:c.795T= ENSP00000497731.1:p.Val265=
ENST00000649902.1:c.795T= ENSP00000497216.1:p.Val265=
ENST00000374855.8:c.795T= ENSP00000363988.4:p.Val265=
ENST00000616752.1:c.795T= ENSP00000481363.1:p.Val265=
NM_000035.3:c.795T= NP_000026.2:p.Val265=
NM_000035.4:c.795T= MANE Select NP_000026.2:p.Val265=