Canonical Allele Identifier: CA589815504
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1228452444
gnomAD v2: 9-104183692-TGCAGC-T
MyVariant Identifiers: chr9:g.104183693_104183697del (hg19) chr9:g.101421411_101421415del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421411_101421415del , CM000671.2:g.101421411_101421415del GRCh38
NC_000009.11:g.104183693_104183697del , CM000671.1:g.104183693_104183697del GRCh37
NC_000009.10:g.103223514_103223518del NCBI36
NG_012387.1:g.19366_19370del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*394_*398del MANE Select ENSP00000497767.1:n.*394_*398del
ENST00000374855.8:c.*394_*398del ENSP00000363988.4:n.*394_*398del
NM_000035.3:c.*394_*398del NP_000026.2:n.*394_*398del
NM_000035.4:c.*394_*398del MANE Select NP_000026.2:n.*394_*398del
Search 100 bp 5'
Search 100 bp 3'