Canonical Allele Identifier: CA5161551

Gene: ALDOB

Linked Data

• dbSNP Id: rs753754412
• ExAC: 9:104188954 C / T
• gnomAD v2: 9-104188954-C-T
• gnomAD v3: 9-101426672-C-T
• gnomAD v4: 9-101426672-C-T
• MyVariant Identifiers: chr9:g.104188954C>T (hg19) ; chr9:g.101426672C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101426672C>T , CM000671.2:g.101426672C>T	GRCh38
NC_000009.11:g.104188954C>T , CM000671.1:g.104188954C>T	GRCh37
NC_000009.10:g.103228775C>T	NCBI36
NG_012387.1:g.14109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.541-34G>A MANE Select	ENSP00000497767.1:n.541-34G>A
ENST00000648064.1:c.541-34G>A	ENSP00000497990.1:n.541-34G>A
ENST00000648758.1:c.541-34G>A	ENSP00000497731.1:n.541-34G>A
ENST00000649902.1:c.541-34G>A	ENSP00000497216.1:n.541-34G>A
ENST00000374855.8:c.541-34G>A	ENSP00000363988.4:n.541-34G>A
ENST00000468981.3:n.68-34G>A
ENST00000616752.1:c.541-34G>A	ENSP00000481363.1:n.541-34G>A
NM_000035.3:c.541-34G>A	NP_000026.2:n.541-34G>A
NM_000035.4:c.541-34G>A MANE Select	NP_000026.2:n.541-34G>A