Canonical Allele Identifier: CA1127396604

Gene: ALDOB

Linked Data

• gnomAD v3: 9-101424759-A-C
• gnomAD v4: 9-101424759-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101424759A>C , CM000671.2:g.101424759A>C	GRCh38
NC_000009.11:g.104187041A>C , CM000671.1:g.104187041A>C	GRCh37
NC_000009.10:g.103226862A>C	NCBI36
NG_012387.1:g.16022T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.999+84T>G MANE Select	ENSP00000497767.1:n.999+84T>G
ENST00000648064.1:c.999+84T>G	ENSP00000497990.1:n.999+84T>G
ENST00000648758.1:c.999+84T>G	ENSP00000497731.1:n.999+84T>G
ENST00000649902.1:c.*54T>G	ENSP00000497216.1:n.*54T>G
ENST00000374855.8:c.999+84T>G	ENSP00000363988.4:n.999+84T>G
ENST00000616752.1:c.*11+84T>G	ENSP00000481363.1:n.*11+84T>G
NM_000035.3:c.999+84T>G	NP_000026.2:n.999+84T>G
NM_000035.4:c.999+84T>G MANE Select	NP_000026.2:n.999+84T>G