Canonical Allele Identifier: CA857733915
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1209544405
MyVariant Identifiers: chr9:g.104191009G>T (hg19) chr9:g.101428727G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101428727G>T , CM000671.2:g.101428727G>T GRCh38
NC_000009.11:g.104191009G>T , CM000671.1:g.104191009G>T GRCh37
NC_000009.10:g.103230830G>T NCBI36
NG_012387.1:g.12054C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.325-204C>A MANE Select ENSP00000497767.1:n.325-204C>A
ENST00000648064.1:c.325-204C>A ENSP00000497990.1:n.325-204C>A
ENST00000648758.1:c.325-204C>A ENSP00000497731.1:n.325-204C>A
ENST00000649902.1:c.325-204C>A ENSP00000497216.1:n.325-204C>A
ENST00000374855.8:c.325-204C>A ENSP00000363988.4:n.325-204C>A
ENST00000468981.3:n.67+1082C>A
ENST00000616752.1:c.325-204C>A ENSP00000481363.1:n.325-204C>A
NM_000035.3:c.325-204C>A NP_000026.2:n.325-204C>A
NM_000035.4:c.325-204C>A MANE Select NP_000026.2:n.325-204C>A
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