Canonical Allele Identifier: CA1868278218
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101424655T= , CM000671.2:g.101424655T= GRCh38
NC_000009.11:g.104186937T= , CM000671.1:g.104186937T= GRCh37
NC_000009.10:g.103226758T= NCBI36
NG_012387.1:g.16126A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.999+188A= MANE Select ENSP00000497767.1:n.999+188A=
ENST00000648064.1:c.999+188A= ENSP00000497990.1:n.999+188A=
ENST00000648758.1:c.999+188A= ENSP00000497731.1:n.999+188A=
ENST00000649902.1:c.*158A= ENSP00000497216.1:n.*158A=
ENST00000374855.8:c.999+188A= ENSP00000363988.4:n.999+188A=
ENST00000616752.1:c.*11+188A= ENSP00000481363.1:n.*11+188A=
NM_000035.3:c.999+188A= NP_000026.2:n.999+188A=
NM_000035.4:c.999+188A= MANE Select NP_000026.2:n.999+188A=