Canonical Allele Identifier: CA918520749
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1564076308
gnomAD v4: 9-101421400-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421406del , CM000671.2:g.101421406del GRCh38
NC_000009.11:g.104183688del , CM000671.1:g.104183688del GRCh37
NC_000009.10:g.103223509del NCBI36
NG_012387.1:g.19380del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*408del MANE Select ENSP00000497767.1:n.*408del
ENST00000374855.8:c.*408del ENSP00000363988.4:n.*408del
NM_000035.3:c.*408del NP_000026.2:n.*408del
NM_000035.4:c.*408del MANE Select NP_000026.2:n.*408del
Search 100 bp 5'
Search 100 bp 3'