Canonical Allele Identifier: CA196955735
Gene: ALDOB HGNC NCBI

Linked Data

dbSNP Id: rs573984819
gnomAD v3: 9-101421688-A-G
gnomAD v4: 9-101421688-A-G
MyVariant Identifiers: chr9:g.104183970A>G (hg19) chr9:g.101421688A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421688A>G , CM000671.2:g.101421688A>G GRCh38
NC_000009.11:g.104183970A>G , CM000671.1:g.104183970A>G GRCh37
NC_000009.10:g.103223791A>G NCBI36
NG_012387.1:g.19093T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*121T>C MANE Select ENSP00000497767.1:n.*121T>C
ENST00000648064.1:c.*121T>C ENSP00000497990.1:n.*121T>C
ENST00000648758.1:c.*121T>C ENSP00000497731.1:n.*121T>C
ENST00000374855.8:c.*121T>C ENSP00000363988.4:n.*121T>C
ENST00000616752.1:c.*228T>C ENSP00000481363.1:n.*228T>C
NM_000035.3:c.*121T>C NP_000026.2:n.*121T>C
NM_000035.4:c.*121T>C MANE Select NP_000026.2:n.*121T>C
Search 100 bp 5'
Search 100 bp 3'