Canonical Allele Identifier: CA466461794
Gene: ALDOB HGNC NCBI

Linked Data

gnomAD v4: 9-101421818-A-G
MyVariant Identifiers: chr9:g.104184100A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421818A>G , CM000671.2:g.101421818A>G GRCh38
NC_000009.11:g.104184100A>G , CM000671.1:g.104184100A>G GRCh37
NC_000009.10:g.103223921A>G NCBI36
NG_012387.1:g.18963T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.1086T>C MANE Select ENSP00000497767.1:p.Tyr362=
ENST00000648064.1:c.1086T>C ENSP00000497990.1:p.Tyr362=
ENST00000648758.1:c.1086T>C ENSP00000497731.1:p.Tyr362=
ENST00000374855.8:c.1086T>C ENSP00000363988.4:p.Tyr362=
ENST00000616752.1:c.*98T>C ENSP00000481363.1:n.*98T>C
NM_000035.3:c.1086T>C NP_000026.2:p.Tyr362=
NM_000035.4:c.1086T>C MANE Select NP_000026.2:p.Tyr362=
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