Canonical Allele Identifier: CA466461840
Gene: ALDOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104184166T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421884T>C , CM000671.2:g.101421884T>C GRCh38
NC_000009.11:g.104184166T>C , CM000671.1:g.104184166T>C GRCh37
NC_000009.10:g.103223987T>C NCBI36
NG_012387.1:g.18897A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1020A>G MANE Select ENSP00000497767.1:p.Lys340=
ENST00000648064.1:c.1020A>G ENSP00000497990.1:p.Lys340=
ENST00000648758.1:c.1020A>G ENSP00000497731.1:p.Lys340=
ENST00000374855.8:c.1020A>G ENSP00000363988.4:p.Lys340=
ENST00000616752.1:c.*32A>G ENSP00000481363.1:n.*32A>G
NM_000035.3:c.1020A>G NP_000026.2:p.Lys340=
NM_000035.4:c.1020A>G MANE Select NP_000026.2:p.Lys340=
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