Canonical Allele Identifier: CA2600889782

Gene: ALDOB

Linked Data

• dbSNP Id: rs1831183779
• gnomAD v3: 9-101429564-G-A
• gnomAD v4: 9-101429564-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429564G>A , CM000671.2:g.101429564G>A	GRCh38
NC_000009.11:g.104191846G>A , CM000671.1:g.104191846G>A	GRCh37
NC_000009.10:g.103231667G>A	NCBI36
NG_012387.1:g.11217C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+191C>T MANE Select	ENSP00000497767.1:n.324+191C>T
ENST00000648064.1:c.324+191C>T	ENSP00000497990.1:n.324+191C>T
ENST00000648758.1:c.324+191C>T	ENSP00000497731.1:n.324+191C>T
ENST00000648906.1:n.685C>T
ENST00000649902.1:c.324+191C>T	ENSP00000497216.1:n.324+191C>T
ENST00000650613.1:n.591C>T
ENST00000374855.8:c.324+191C>T	ENSP00000363988.4:n.324+191C>T
ENST00000468981.3:n.67+245C>T
ENST00000616752.1:c.324+191C>T	ENSP00000481363.1:n.324+191C>T
NM_000035.3:c.324+191C>T	NP_000026.2:n.324+191C>T
NM_000035.4:c.324+191C>T MANE Select	NP_000026.2:n.324+191C>T