Canonical Allele Identifier: CA196955627
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs949099709
gnomAD v2: 9-104183717-C-T
gnomAD v3: 9-101421435-C-T
gnomAD v4: 9-101421435-C-T
MyVariant Identifiers: chr9:g.104183717C>T (hg19) chr9:g.101421435C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421435C>T , CM000671.2:g.101421435C>T GRCh38
NC_000009.11:g.104183717C>T , CM000671.1:g.104183717C>T GRCh37
NC_000009.10:g.103223538C>T NCBI36
NG_012387.1:g.19346G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*374G>A MANE Select ENSP00000497767.1:n.*374G>A
ENST00000374855.8:c.*374G>A ENSP00000363988.4:n.*374G>A
NM_000035.3:c.*374G>A NP_000026.2:n.*374G>A
NM_000035.4:c.*374G>A MANE Select NP_000026.2:n.*374G>A
Search 100 bp 5'
Search 100 bp 3'