Canonical Allele Identifier: CA466461852
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1012065747
MyVariant Identifiers: chr9:g.104184194A>G (hg19) chr9:g.101421912A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421912A>G , CM000671.2:g.101421912A>G GRCh38
NC_000009.11:g.104184194A>G , CM000671.1:g.104184194A>G GRCh37
NC_000009.10:g.103224015A>G NCBI36
NG_012387.1:g.18869T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1000-8T>C MANE Select ENSP00000497767.1:n.1000-8T>C
ENST00000648064.1:c.1000-8T>C ENSP00000497990.1:n.1000-8T>C
ENST00000648758.1:c.1000-8T>C ENSP00000497731.1:n.1000-8T>C
ENST00000374855.8:c.1000-8T>C ENSP00000363988.4:n.1000-8T>C
ENST00000616752.1:c.*12-8T>C ENSP00000481363.1:n.*12-8T>C
NM_000035.3:c.1000-8T>C NP_000026.2:n.1000-8T>C
NM_000035.4:c.1000-8T>C MANE Select NP_000026.2:n.1000-8T>C
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