Canonical Allele Identifier: CA466461837
Gene: ALDOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104184163T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421881T>A , CM000671.2:g.101421881T>A GRCh38
NC_000009.11:g.104184163T>A , CM000671.1:g.104184163T>A GRCh37
NC_000009.10:g.103223984T>A NCBI36
NG_012387.1:g.18900A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1023A>T MANE Select ENSP00000497767.1:p.Gly341=
ENST00000648064.1:c.1023A>T ENSP00000497990.1:p.Gly341=
ENST00000648758.1:c.1023A>T ENSP00000497731.1:p.Gly341=
ENST00000374855.8:c.1023A>T ENSP00000363988.4:p.Gly341=
ENST00000616752.1:c.*35A>T ENSP00000481363.1:n.*35A>T
NM_000035.3:c.1023A>T NP_000026.2:p.Gly341=
NM_000035.4:c.1023A>T MANE Select NP_000026.2:p.Gly341=
Search 100 bp 5'
Search 100 bp 3'