Canonical Allele Identifier: CA1868275231
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421484A= , CM000671.2:g.101421484A= GRCh38
NC_000009.11:g.104183766A= , CM000671.1:g.104183766A= GRCh37
NC_000009.10:g.103223587A= NCBI36
NG_012387.1:g.19297T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*325T= MANE Select ENSP00000497767.1:n.*325T=
ENST00000648064.1:c.*325T= ENSP00000497990.1:n.*325T=
ENST00000374855.8:c.*325T= ENSP00000363988.4:n.*325T=
NM_000035.3:c.*325T= NP_000026.2:n.*325T=
NM_000035.4:c.*325T= MANE Select NP_000026.2:n.*325T=