Canonical Allele Identifier: CA196957970

Gene: ALDOB

Linked Data

• dbSNP Id: rs952210869
• gnomAD v2: 9-104191880-G-T
• gnomAD v3: 9-101429598-G-T
• gnomAD v4: 9-101429598-G-T
• MyVariant Identifiers: chr9:g.104191880G>T (hg19) ; chr9:g.101429598G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101429598G>T , CM000671.2:g.101429598G>T	GRCh38
NC_000009.11:g.104191880G>T , CM000671.1:g.104191880G>T	GRCh37
NC_000009.10:g.103231701G>T	NCBI36
NG_012387.1:g.11183C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.324+157C>A MANE Select	ENSP00000497767.1:n.324+157C>A
ENST00000648064.1:c.324+157C>A	ENSP00000497990.1:n.324+157C>A
ENST00000648758.1:c.324+157C>A	ENSP00000497731.1:n.324+157C>A
ENST00000648906.1:n.651C>A
ENST00000649902.1:c.324+157C>A	ENSP00000497216.1:n.324+157C>A
ENST00000650613.1:n.557C>A
ENST00000374855.8:c.324+157C>A	ENSP00000363988.4:n.324+157C>A
ENST00000468981.3:n.67+211C>A
ENST00000616752.1:c.324+157C>A	ENSP00000481363.1:n.324+157C>A
NM_000035.3:c.324+157C>A	NP_000026.2:n.324+157C>A
NM_000035.4:c.324+157C>A MANE Select	NP_000026.2:n.324+157C>A