Canonical Allele Identifier: CA589815510
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs1472415117
gnomAD v2: 9-104183744-A-C
gnomAD v3: 9-101421462-A-C
gnomAD v4: 9-101421462-A-C
MyVariant Identifiers: chr9:g.104183744A>C (hg19) chr9:g.101421462A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421462A>C , CM000671.2:g.101421462A>C GRCh38
NC_000009.11:g.104183744A>C , CM000671.1:g.104183744A>C GRCh37
NC_000009.10:g.103223565A>C NCBI36
NG_012387.1:g.19319T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*347T>G MANE Select ENSP00000497767.1:n.*347T>G
ENST00000648064.1:c.*347T>G ENSP00000497990.1:n.*347T>G
ENST00000374855.8:c.*347T>G ENSP00000363988.4:n.*347T>G
NM_000035.3:c.*347T>G NP_000026.2:n.*347T>G
NM_000035.4:c.*347T>G MANE Select NP_000026.2:n.*347T>G
Search 100 bp 5'
Search 100 bp 3'