Canonical Allele Identifier: CA196955606
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1054937198
gnomAD v4: 9-101421386-T-C
MyVariant Identifiers: chr9:g.104183668T>C (hg19) chr9:g.101421386T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421386T>C , CM000671.2:g.101421386T>C GRCh38
NC_000009.11:g.104183668T>C , CM000671.1:g.104183668T>C GRCh37
NC_000009.10:g.103223489T>C NCBI36
NG_012387.1:g.19395A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*423A>G MANE Select ENSP00000497767.1:n.*423A>G
ENST00000374855.8:c.*423A>G ENSP00000363988.4:n.*423A>G
NM_000035.3:c.*423A>G NP_000026.2:n.*423A>G
NM_000035.4:c.*423A>G MANE Select NP_000026.2:n.*423A>G
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Search 100 bp 3'