Canonical Allele Identifier: CA196955680
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1005924855
gnomAD v2: 9-104183833-TG-T
gnomAD v3: 9-101421551-TG-T
gnomAD v4: 9-101421551-TG-T
MyVariant Identifiers: chr9:g.104183834del (hg19) chr9:g.101421552del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421554del , CM000671.2:g.101421554del GRCh38
NC_000009.11:g.104183836del , CM000671.1:g.104183836del GRCh37
NC_000009.10:g.103223657del NCBI36
NG_012387.1:g.19229del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*257del MANE Select ENSP00000497767.1:n.*257del
ENST00000648064.1:c.*257del ENSP00000497990.1:n.*257del
ENST00000374855.8:c.*257del ENSP00000363988.4:n.*257del
ENST00000616752.1:c.*364del ENSP00000481363.1:n.*364del
NM_000035.3:c.*257del NP_000026.2:n.*257del
NM_000035.4:c.*257del MANE Select NP_000026.2:n.*257del
Search 100 bp 5'
Search 100 bp 3'