Canonical Allele Identifier: CA590045523

Gene: ALDOB

Linked Data

• dbSNP Id: rs1369589867
• gnomAD v2: 9-104187099-G-A
• gnomAD v4: 9-101424817-G-A
• MyVariant Identifiers: chr9:g.104187099G>A (hg19) ; chr9:g.101424817G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424817G>A , CM000671.2:g.101424817G>A	GRCh38
NC_000009.11:g.104187099G>A , CM000671.1:g.104187099G>A	GRCh37
NC_000009.10:g.103226920G>A	NCBI36
NG_012387.1:g.15964C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.999+26C>T MANE Select	ENSP00000497767.1:n.999+26C>T
ENST00000648064.1:c.999+26C>T	ENSP00000497990.1:n.999+26C>T
ENST00000648758.1:c.999+26C>T	ENSP00000497731.1:n.999+26C>T
ENST00000649902.1:c.1025C>T	ENSP00000497216.1:p.Thr342Ile
ENST00000374855.8:c.999+26C>T	ENSP00000363988.4:n.999+26C>T
ENST00000616752.1:c.*11+26C>T	ENSP00000481363.1:n.*11+26C>T
NM_000035.3:c.999+26C>T	NP_000026.2:n.999+26C>T
NM_000035.4:c.999+26C>T MANE Select	NP_000026.2:n.999+26C>T