Canonical Allele Identifier: CA1868275247
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421517G= , CM000671.2:g.101421517G= GRCh38
NC_000009.11:g.104183799G= , CM000671.1:g.104183799G= GRCh37
NC_000009.10:g.103223620G= NCBI36
NG_012387.1:g.19264C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*292C= MANE Select ENSP00000497767.1:n.*292C=
ENST00000648064.1:c.*292C= ENSP00000497990.1:n.*292C=
ENST00000374855.8:c.*292C= ENSP00000363988.4:n.*292C=
NM_000035.3:c.*292C= NP_000026.2:n.*292C=
NM_000035.4:c.*292C= MANE Select NP_000026.2:n.*292C=