Canonical Allele Identifier: CA196955683
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs555823408
gnomAD v3: 9-101421575-G-T
gnomAD v4: 9-101421575-G-T
MyVariant Identifiers: chr9:g.104183857G>T (hg19) chr9:g.101421575G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421575G>T , CM000671.2:g.101421575G>T GRCh38
NC_000009.11:g.104183857G>T , CM000671.1:g.104183857G>T GRCh37
NC_000009.10:g.103223678G>T NCBI36
NG_012387.1:g.19206C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*234C>A MANE Select ENSP00000497767.1:n.*234C>A
ENST00000648064.1:c.*234C>A ENSP00000497990.1:n.*234C>A
ENST00000374855.8:c.*234C>A ENSP00000363988.4:n.*234C>A
ENST00000616752.1:c.*341C>A ENSP00000481363.1:n.*341C>A
NM_000035.3:c.*234C>A NP_000026.2:n.*234C>A
NM_000035.4:c.*234C>A MANE Select NP_000026.2:n.*234C>A
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