Canonical Allele Identifier: CA590045536

Gene: ALDOB

Linked Data

• dbSNP Id: rs1364133544
• gnomAD v2: 9-104187489-G-C
• gnomAD v3: 9-101425207-G-C
• gnomAD v4: 9-101425207-G-C
• MyVariant Identifiers: chr9:g.104187489G>C (hg19) ; chr9:g.101425207G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425207G>C , CM000671.2:g.101425207G>C	GRCh38
NC_000009.11:g.104187489G>C , CM000671.1:g.104187489G>C	GRCh37
NC_000009.10:g.103227310G>C	NCBI36
NG_012387.1:g.15574C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.800-165C>G MANE Select	ENSP00000497767.1:n.800-165C>G
ENST00000648064.1:c.800-165C>G	ENSP00000497990.1:n.800-165C>G
ENST00000648758.1:c.800-165C>G	ENSP00000497731.1:n.800-165C>G
ENST00000649902.1:c.800-165C>G	ENSP00000497216.1:n.800-165C>G
ENST00000374855.8:c.800-165C>G	ENSP00000363988.4:n.800-165C>G
ENST00000616752.1:c.800-165C>G	ENSP00000481363.1:n.800-165C>G
NM_000035.3:c.800-165C>G	NP_000026.2:n.800-165C>G
NM_000035.4:c.800-165C>G MANE Select	NP_000026.2:n.800-165C>G