Canonical Allele Identifier: CA196956813

Gene: ALDOB

Linked Data

• ClinVar Variation Id: 2315682
• ClinVar RCV Id: RCV002919348
• dbSNP Id: rs1055615924
• gnomAD v2: 9-104187840-T-C
• gnomAD v4: 9-101425558-T-C
• MyVariant Identifiers: chr9:g.104187840T>C (hg19) ; chr9:g.101425558T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425558T>C , CM000671.2:g.101425558T>C	GRCh38
NC_000009.11:g.104187840T>C , CM000671.1:g.104187840T>C	GRCh37
NC_000009.10:g.103227661T>C	NCBI36
NG_012387.1:g.15223A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.694A>G MANE Select	ENSP00000497767.1:p.Asn232Asp
ENST00000648064.1:c.694A>G	ENSP00000497990.1:p.Asn232Asp
ENST00000648758.1:c.694A>G	ENSP00000497731.1:p.Asn232Asp
ENST00000649902.1:c.694A>G	ENSP00000497216.1:p.Asn232Asp
ENST00000374855.8:c.694A>G	ENSP00000363988.4:p.Asn232Asp
ENST00000616752.1:c.694A>G	ENSP00000481363.1:p.Asn232Asp
NM_000035.3:c.694A>G	NP_000026.2:p.Asn232Asp
NM_000035.4:c.694A>G MANE Select	NP_000026.2:p.Asn232Asp