Canonical Allele Identifier: CA466462110
Gene: ALDOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104187856G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425574G>C , CM000671.2:g.101425574G>C GRCh38
NC_000009.11:g.104187856G>C , CM000671.1:g.104187856G>C GRCh37
NC_000009.10:g.103227677G>C NCBI36
NG_012387.1:g.15207C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.678C>G MANE Select ENSP00000497767.1:p.Gly226=
ENST00000648064.1:c.678C>G ENSP00000497990.1:p.Gly226=
ENST00000648758.1:c.678C>G ENSP00000497731.1:p.Gly226=
ENST00000649902.1:c.678C>G ENSP00000497216.1:p.Gly226=
ENST00000374855.8:c.678C>G ENSP00000363988.4:p.Gly226=
ENST00000468981.3:n.205C>G
ENST00000616752.1:c.678C>G ENSP00000481363.1:p.Gly226=
NM_000035.3:c.678C>G NP_000026.2:p.Gly226=
NM_000035.4:c.678C>G MANE Select NP_000026.2:p.Gly226=
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