Canonical Allele Identifier: CA196955621
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs773210631
MyVariant Identifiers: chr9:g.104183716del (hg19) chr9:g.101421434del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421435del , CM000671.2:g.101421435del GRCh38
NC_000009.11:g.104183717del , CM000671.1:g.104183717del GRCh37
NC_000009.10:g.103223538del NCBI36
NG_012387.1:g.19347del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*375del MANE Select ENSP00000497767.1:n.*375del
ENST00000374855.8:c.*375del ENSP00000363988.4:n.*375del
NM_000035.3:c.*375del NP_000026.2:n.*375del
NM_000035.4:c.*375del MANE Select NP_000026.2:n.*375del
Search 100 bp 5'
Search 100 bp 3'