Canonical Allele Identifier: CA1868275766
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421906T= , CM000671.2:g.101421906T= GRCh38
NC_000009.11:g.104184188T= , CM000671.1:g.104184188T= GRCh37
NC_000009.10:g.103224009T= NCBI36
NG_012387.1:g.18875A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1000-2A= MANE Select ENSP00000497767.1:n.1000-2A=
ENST00000648064.1:c.1000-2A= ENSP00000497990.1:n.1000-2A=
ENST00000648758.1:c.1000-2A= ENSP00000497731.1:n.1000-2A=
ENST00000374855.8:c.1000-2A= ENSP00000363988.4:n.1000-2A=
ENST00000616752.1:c.*12-2A= ENSP00000481363.1:n.*12-2A=
NM_000035.3:c.1000-2A= NP_000026.2:n.1000-2A=
NM_000035.4:c.1000-2A= MANE Select NP_000026.2:n.1000-2A=