Canonical Allele Identifier: CA857728561

Gene: ALDOB

Linked Data

• dbSNP Id: rs1300916507
• gnomAD v4: 9-101421715-C-A
• MyVariant Identifiers: chr9:g.104183997C>A (hg19) ; chr9:g.101421715C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421715C>A , CM000671.2:g.101421715C>A	GRCh38
NC_000009.11:g.104183997C>A , CM000671.1:g.104183997C>A	GRCh37
NC_000009.10:g.103223818C>A	NCBI36
NG_012387.1:g.19066G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.*94G>T MANE Select	ENSP00000497767.1:n.*94G>T
ENST00000648064.1:c.*94G>T	ENSP00000497990.1:n.*94G>T
ENST00000648758.1:c.*94G>T	ENSP00000497731.1:n.*94G>T
ENST00000374855.8:c.*94G>T	ENSP00000363988.4:n.*94G>T
ENST00000616752.1:c.*201G>T	ENSP00000481363.1:n.*201G>T
NM_000035.3:c.*94G>T	NP_000026.2:n.*94G>T
NM_000035.4:c.*94G>T MANE Select	NP_000026.2:n.*94G>T