Canonical Allele Identifier: CA1868279182
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425649C= , CM000671.2:g.101425649C= GRCh38
NC_000009.11:g.104187931C= , CM000671.1:g.104187931C= GRCh37
NC_000009.10:g.103227752C= NCBI36
NG_012387.1:g.15132G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.625-22G= MANE Select ENSP00000497767.1:n.625-22G=
ENST00000648064.1:c.625-22G= ENSP00000497990.1:n.625-22G=
ENST00000648758.1:c.625-22G= ENSP00000497731.1:n.625-22G=
ENST00000649902.1:c.625-22G= ENSP00000497216.1:n.625-22G=
ENST00000374855.8:c.625-22G= ENSP00000363988.4:n.625-22G=
ENST00000468981.3:n.152-22G=
ENST00000616752.1:c.625-22G= ENSP00000481363.1:n.625-22G=
NM_000035.3:c.625-22G= NP_000026.2:n.625-22G=
NM_000035.4:c.625-22G= MANE Select NP_000026.2:n.625-22G=