Canonical Allele Identifier: CA196958028
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1617538
ClinVar RCV Id: RCV002079323
dbSNP Id: rs561489667
gnomAD v3: 9-101429764-C-T
gnomAD v4: 9-101429764-C-T
MyVariant Identifiers: chr9:g.104192046C>T (hg19) chr9:g.101429764C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429764C>T , CM000671.2:g.101429764C>T GRCh38
NC_000009.11:g.104192046C>T , CM000671.1:g.104192046C>T GRCh37
NC_000009.10:g.103231867C>T NCBI36
NG_012387.1:g.11017G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.315G>A MANE Select ENSP00000497767.1:p.Val105=
ENST00000648064.1:c.315G>A ENSP00000497990.1:p.Val105=
ENST00000648758.1:c.315G>A ENSP00000497731.1:p.Val105=
ENST00000648906.1:n.485G>A
ENST00000649902.1:c.315G>A ENSP00000497216.1:p.Val105=
ENST00000650613.1:n.391G>A
ENST00000374855.8:c.315G>A ENSP00000363988.4:p.Val105=
ENST00000468981.3:n.67+45G>A
ENST00000616752.1:c.315G>A ENSP00000481363.1:p.Val105=
NM_000035.3:c.315G>A NP_000026.2:p.Val105=
NM_000035.4:c.315G>A MANE Select NP_000026.2:p.Val105=
Search 100 bp 5'
Search 100 bp 3'