Canonical Allele Identifier: CA589815509
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1564076335
gnomAD v2: 9-104183730-G-GT
gnomAD v3: 9-101421448-G-GT
gnomAD v4: 9-101421448-G-GT
MyVariant Identifiers: chr9:g.104183730_104183731insT (hg19) chr9:g.101421448_101421449insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421451dup , CM000671.2:g.101421451dup GRCh38
NC_000009.11:g.104183733dup , CM000671.1:g.104183733dup GRCh37
NC_000009.10:g.103223554dup NCBI36
NG_012387.1:g.19332dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*360dup MANE Select ENSP00000497767.1:n.*360dup
ENST00000648064.1:c.*360dup ENSP00000497990.1:n.*360dup
ENST00000374855.8:c.*360dup ENSP00000363988.4:n.*360dup
NM_000035.3:c.*360dup NP_000026.2:n.*360dup
NM_000035.4:c.*360dup MANE Select NP_000026.2:n.*360dup
Search 100 bp 5'
Search 100 bp 3'