Canonical Allele Identifier: CA466462844

Gene: ALDOB

Linked Data

• ClinVar Variation Id: 1604764
• ClinVar RCV Id: RCV002159867
• dbSNP Id: rs1831133410
• MyVariant Identifiers: chr9:g.104188914G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101426632G>A , CM000671.2:g.101426632G>A	GRCh38
NC_000009.11:g.104188914G>A , CM000671.1:g.104188914G>A	GRCh37
NC_000009.10:g.103228735G>A	NCBI36
NG_012387.1:g.14149C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.547C>T MANE Select	ENSP00000497767.1:p.Leu183=
ENST00000648064.1:c.547C>T	ENSP00000497990.1:p.Leu183=
ENST00000648758.1:c.547C>T	ENSP00000497731.1:p.Leu183=
ENST00000649902.1:c.547C>T	ENSP00000497216.1:p.Leu183=
ENST00000374855.8:c.547C>T	ENSP00000363988.4:p.Leu183=
ENST00000468981.3:n.74C>T
ENST00000616752.1:c.547C>T	ENSP00000481363.1:p.Leu183=
NM_000035.3:c.547C>T	NP_000026.2:p.Leu183=
NM_000035.4:c.547C>T MANE Select	NP_000026.2:p.Leu183=