Canonical Allele Identifier: CA374266135

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104193082T>C (hg19) ; chr9:g.101430800T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430800T>C , CM000671.2:g.101430800T>C	GRCh38
NC_000009.11:g.104193082T>C , CM000671.1:g.104193082T>C	GRCh37
NC_000009.10:g.103232903T>C	NCBI36
NG_012387.1:g.9981A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.88A>G MANE Select	ENSP00000497767.1:p.Ile30Val
ENST00000648064.1:c.88A>G	ENSP00000497990.1:p.Ile30Val
ENST00000648423.1:c.88A>G	ENSP00000497985.1:p.Ile30Val
ENST00000648758.1:c.88A>G	ENSP00000497731.1:p.Ile30Val
ENST00000648906.1:n.258A>G
ENST00000649902.1:c.88A>G	ENSP00000497216.1:p.Ile30Val
ENST00000650613.1:n.164A>G
ENST00000374855.8:c.88A>G	ENSP00000363988.4:p.Ile30Val
ENST00000616752.1:c.88A>G	ENSP00000481363.1:p.Ile30Val
NM_000035.3:c.88A>G	NP_000026.2:p.Ile30Val
NM_000035.4:c.88A>G MANE Select	NP_000026.2:p.Ile30Val