Canonical Allele Identifier: CA2691007155
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2978919
ClinVar RCV Id: RCV003839565
gnomAD v4: 9-101425437-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425437A>G , CM000671.2:g.101425437A>G GRCh38
NC_000009.11:g.104187719A>G , CM000671.1:g.104187719A>G GRCh37
NC_000009.10:g.103227540A>G NCBI36
NG_012387.1:g.15344T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.799+16T>C MANE Select ENSP00000497767.1:n.799+16T>C
ENST00000648064.1:c.799+16T>C ENSP00000497990.1:n.799+16T>C
ENST00000648758.1:c.799+16T>C ENSP00000497731.1:n.799+16T>C
ENST00000649902.1:c.799+16T>C ENSP00000497216.1:n.799+16T>C
ENST00000374855.8:c.799+16T>C ENSP00000363988.4:n.799+16T>C
ENST00000616752.1:c.799+16T>C ENSP00000481363.1:n.799+16T>C
NM_000035.3:c.799+16T>C NP_000026.2:n.799+16T>C
NM_000035.4:c.799+16T>C MANE Select NP_000026.2:n.799+16T>C
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