Canonical Allele Identifier: CA1868278307

Gene: ALDOB

Linked Data

• dbSNP Id: rs1831097132
• gnomAD v4: 9-101424755-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424755G>C , CM000671.2:g.101424755G>C	GRCh38
NC_000009.11:g.104187037G>C , CM000671.1:g.104187037G>C	GRCh37
NC_000009.10:g.103226858G>C	NCBI36
NG_012387.1:g.16026C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.999+88C>G MANE Select	ENSP00000497767.1:n.999+88C>G
ENST00000648064.1:c.999+88C>G	ENSP00000497990.1:n.999+88C>G
ENST00000648758.1:c.999+88C>G	ENSP00000497731.1:n.999+88C>G
ENST00000649902.1:c.*58C>G	ENSP00000497216.1:n.*58C>G
ENST00000374855.8:c.999+88C>G	ENSP00000363988.4:n.999+88C>G
ENST00000616752.1:c.*11+88C>G	ENSP00000481363.1:n.*11+88C>G
NM_000035.3:c.999+88C>G	NP_000026.2:n.999+88C>G
NM_000035.4:c.999+88C>G MANE Select	NP_000026.2:n.999+88C>G