Canonical Allele Identifier: CA589815520

Gene: ALDOB

Linked Data

• dbSNP Id: rs564274420
• gnomAD v2: 9-104184081-G-C
• gnomAD v3: 9-101421799-G-C
• gnomAD v4: 9-101421799-G-C
• MyVariant Identifiers: chr9:g.104184081G>C (hg19) ; chr9:g.101421799G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421799G>C , CM000671.2:g.101421799G>C	GRCh38
NC_000009.11:g.104184081G>C , CM000671.1:g.104184081G>C	GRCh37
NC_000009.10:g.103223902G>C	NCBI36
NG_012387.1:g.18982C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.*10C>G MANE Select	ENSP00000497767.1:n.*10C>G
ENST00000648064.1:c.*10C>G	ENSP00000497990.1:n.*10C>G
ENST00000648758.1:c.*10C>G	ENSP00000497731.1:n.*10C>G
ENST00000374855.8:c.*10C>G	ENSP00000363988.4:n.*10C>G
ENST00000616752.1:c.*117C>G	ENSP00000481363.1:n.*117C>G
NM_000035.3:c.*10C>G	NP_000026.2:n.*10C>G
NM_000035.4:c.*10C>G MANE Select	NP_000026.2:n.*10C>G