Canonical Allele Identifier: CA374266076

Gene: ALDOB

Linked Data

• ClinVar Variation Id: 2107734
• ClinVar RCV Id: RCV003033790
• MyVariant Identifiers: chr9:g.104192250T>C (hg19) ; chr9:g.101429968T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429968T>C , CM000671.2:g.101429968T>C	GRCh38
NC_000009.11:g.104192250T>C , CM000671.1:g.104192250T>C	GRCh37
NC_000009.10:g.103232071T>C	NCBI36
NG_012387.1:g.10813A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.113-2A>G MANE Select	ENSP00000497767.1:n.113-2A>G
ENST00000648064.1:c.113-2A>G	ENSP00000497990.1:n.113-2A>G
ENST00000648423.1:c.113-2A>G	ENSP00000497985.1:n.113-2A>G
ENST00000648758.1:c.113-2A>G	ENSP00000497731.1:n.113-2A>G
ENST00000648906.1:n.283-2A>G
ENST00000649902.1:c.113-2A>G	ENSP00000497216.1:n.113-2A>G
ENST00000650613.1:n.189-2A>G
ENST00000374855.8:c.113-2A>G	ENSP00000363988.4:n.113-2A>G
ENST00000616752.1:c.113-2A>G	ENSP00000481363.1:n.113-2A>G
NM_000035.3:c.113-2A>G	NP_000026.2:n.113-2A>G
NM_000035.4:c.113-2A>G MANE Select	NP_000026.2:n.113-2A>G