Canonical Allele Identifier: CA1868275204
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421452C= , CM000671.2:g.101421452C= GRCh38
NC_000009.11:g.104183734C= , CM000671.1:g.104183734C= GRCh37
NC_000009.10:g.103223555C= NCBI36
NG_012387.1:g.19329G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*357G= MANE Select ENSP00000497767.1:n.*357G=
ENST00000648064.1:c.*357G= ENSP00000497990.1:n.*357G=
ENST00000374855.8:c.*357G= ENSP00000363988.4:n.*357G=
NM_000035.3:c.*357G= NP_000026.2:n.*357G=
NM_000035.4:c.*357G= MANE Select NP_000026.2:n.*357G=