Canonical Allele Identifier: CA196956818

Gene: ALDOB

Linked Data

• dbSNP Id: rs371219301
• gnomAD v3: 9-101425572-G-A
• gnomAD v4: 9-101425572-G-A
• MyVariant Identifiers: chr9:g.104187854G>A (hg19) ; chr9:g.101425572G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425572G>A , CM000671.2:g.101425572G>A	GRCh38
NC_000009.11:g.104187854G>A , CM000671.1:g.104187854G>A	GRCh37
NC_000009.10:g.103227675G>A	NCBI36
NG_012387.1:g.15209C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.680C>T MANE Select	ENSP00000497767.1:p.Thr227Ile
ENST00000648064.1:c.680C>T	ENSP00000497990.1:p.Thr227Ile
ENST00000648758.1:c.680C>T	ENSP00000497731.1:p.Thr227Ile
ENST00000649902.1:c.680C>T	ENSP00000497216.1:p.Thr227Ile
ENST00000374855.8:c.680C>T	ENSP00000363988.4:p.Thr227Ile
ENST00000468981.3:n.207C>T
ENST00000616752.1:c.680C>T	ENSP00000481363.1:p.Thr227Ile
NM_000035.3:c.680C>T	NP_000026.2:p.Thr227Ile
NM_000035.4:c.680C>T MANE Select	NP_000026.2:p.Thr227Ile