Canonical Allele Identifier: CA1868278362
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101424812A= , CM000671.2:g.101424812A= GRCh38
NC_000009.11:g.104187094A= , CM000671.1:g.104187094A= GRCh37
NC_000009.10:g.103226915A= NCBI36
NG_012387.1:g.15969T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.999+31T= MANE Select ENSP00000497767.1:n.999+31T=
ENST00000648064.1:c.999+31T= ENSP00000497990.1:n.999+31T=
ENST00000648758.1:c.999+31T= ENSP00000497731.1:n.999+31T=
ENST00000649902.1:c.*1T= ENSP00000497216.1:n.*1T=
ENST00000374855.8:c.999+31T= ENSP00000363988.4:n.999+31T=
ENST00000616752.1:c.*11+31T= ENSP00000481363.1:n.*11+31T=
NM_000035.3:c.999+31T= NP_000026.2:n.999+31T=
NM_000035.4:c.999+31T= MANE Select NP_000026.2:n.999+31T=
Search 100 bp 5'
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