Canonical Allele Identifier: CA590045541
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1369838863
gnomAD v2: 9-104189721-AC-A
gnomAD v4: 9-101427439-AC-A
MyVariant Identifiers: chr9:g.104189722del (hg19) chr9:g.101427440del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101427440del , CM000671.2:g.101427440del GRCh38
NC_000009.11:g.104189722del , CM000671.1:g.104189722del GRCh37
NC_000009.10:g.103229543del NCBI36
NG_012387.1:g.13341del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.540+42del MANE Select ENSP00000497767.1:n.540+42del
ENST00000648064.1:c.540+42del ENSP00000497990.1:n.540+42del
ENST00000648758.1:c.540+42del ENSP00000497731.1:n.540+42del
ENST00000649902.1:c.540+42del ENSP00000497216.1:n.540+42del
ENST00000374855.8:c.540+42del ENSP00000363988.4:n.540+42del
ENST00000468981.3:n.68-802del
ENST00000616752.1:c.540+42del ENSP00000481363.1:n.540+42del
NM_000035.3:c.540+42del NP_000026.2:n.540+42del
NM_000035.4:c.540+42del MANE Select NP_000026.2:n.540+42del
Search 100 bp 5'
Search 100 bp 3'