Canonical Allele Identifier: CA1868280995
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429533T= , CM000671.2:g.101429533T= GRCh38
NC_000009.11:g.104191815T= , CM000671.1:g.104191815T= GRCh37
NC_000009.10:g.103231636T= NCBI36
NG_012387.1:g.11248A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.324+222A= MANE Select ENSP00000497767.1:n.324+222A=
ENST00000648064.1:c.324+222A= ENSP00000497990.1:n.324+222A=
ENST00000648758.1:c.324+222A= ENSP00000497731.1:n.324+222A=
ENST00000648906.1:n.716A=
ENST00000649902.1:c.324+222A= ENSP00000497216.1:n.324+222A=
ENST00000650613.1:n.622A=
ENST00000374855.8:c.324+222A= ENSP00000363988.4:n.324+222A=
ENST00000468981.3:n.67+276A=
ENST00000616752.1:c.324+222A= ENSP00000481363.1:n.324+222A=
NM_000035.3:c.324+222A= NP_000026.2:n.324+222A=
NM_000035.4:c.324+222A= MANE Select NP_000026.2:n.324+222A=
Search 100 bp 5'
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