Canonical Allele Identifier: CA1868278348
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101424798C= , CM000671.2:g.101424798C= GRCh38
NC_000009.11:g.104187080C= , CM000671.1:g.104187080C= GRCh37
NC_000009.10:g.103226901C= NCBI36
NG_012387.1:g.15983G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.999+45G= MANE Select ENSP00000497767.1:n.999+45G=
ENST00000648064.1:c.999+45G= ENSP00000497990.1:n.999+45G=
ENST00000648758.1:c.999+45G= ENSP00000497731.1:n.999+45G=
ENST00000649902.1:c.*15G= ENSP00000497216.1:n.*15G=
ENST00000374855.8:c.999+45G= ENSP00000363988.4:n.999+45G=
ENST00000616752.1:c.*11+45G= ENSP00000481363.1:n.*11+45G=
NM_000035.3:c.999+45G= NP_000026.2:n.999+45G=
NM_000035.4:c.999+45G= MANE Select NP_000026.2:n.999+45G=
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