Canonical Allele Identifier: CA1868275438
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421712A= , CM000671.2:g.101421712A= GRCh38
NC_000009.11:g.104183994A= , CM000671.1:g.104183994A= GRCh37
NC_000009.10:g.103223815A= NCBI36
NG_012387.1:g.19069T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*97T= MANE Select ENSP00000497767.1:n.*97T=
ENST00000648064.1:c.*97T= ENSP00000497990.1:n.*97T=
ENST00000648758.1:c.*97T= ENSP00000497731.1:n.*97T=
ENST00000374855.8:c.*97T= ENSP00000363988.4:n.*97T=
ENST00000616752.1:c.*204T= ENSP00000481363.1:n.*204T=
NM_000035.3:c.*97T= NP_000026.2:n.*97T=
NM_000035.4:c.*97T= MANE Select NP_000026.2:n.*97T=