Canonical Allele Identifier: CA1868275203
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421449T= , CM000671.2:g.101421449T= GRCh38
NC_000009.11:g.104183731T= , CM000671.1:g.104183731T= GRCh37
NC_000009.10:g.103223552T= NCBI36
NG_012387.1:g.19332A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*360A= MANE Select ENSP00000497767.1:n.*360A=
ENST00000648064.1:c.*360A= ENSP00000497990.1:n.*360A=
ENST00000374855.8:c.*360A= ENSP00000363988.4:n.*360A=
NM_000035.3:c.*360A= NP_000026.2:n.*360A=
NM_000035.4:c.*360A= MANE Select NP_000026.2:n.*360A=