Canonical Allele Identifier: CA1868275501
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421768C= , CM000671.2:g.101421768C= GRCh38
NC_000009.11:g.104184050C= , CM000671.1:g.104184050C= GRCh37
NC_000009.10:g.103223871C= NCBI36
NG_012387.1:g.19013G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*41G= MANE Select ENSP00000497767.1:n.*41G=
ENST00000648064.1:c.*41G= ENSP00000497990.1:n.*41G=
ENST00000648758.1:c.*41G= ENSP00000497731.1:n.*41G=
ENST00000374855.8:c.*41G= ENSP00000363988.4:n.*41G=
ENST00000616752.1:c.*148G= ENSP00000481363.1:n.*148G=
NM_000035.3:c.*41G= NP_000026.2:n.*41G=
NM_000035.4:c.*41G= MANE Select NP_000026.2:n.*41G=
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