Canonical Allele Identifier: CA1868275568
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421802T= , CM000671.2:g.101421802T= GRCh38
NC_000009.11:g.104184084T= , CM000671.1:g.104184084T= GRCh37
NC_000009.10:g.103223905T= NCBI36
NG_012387.1:g.18979A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*7A= MANE Select ENSP00000497767.1:n.*7A=
ENST00000648064.1:c.*7A= ENSP00000497990.1:n.*7A=
ENST00000648758.1:c.*7A= ENSP00000497731.1:n.*7A=
ENST00000374855.8:c.*7A= ENSP00000363988.4:n.*7A=
ENST00000616752.1:c.*114A= ENSP00000481363.1:n.*114A=
NM_000035.3:c.*7A= NP_000026.2:n.*7A=
NM_000035.4:c.*7A= MANE Select NP_000026.2:n.*7A=