Canonical Allele Identifier: CA466462195

Gene: ALDOB

Linked Data

• dbSNP Id: rs1338499743
• gnomAD v2: 9-104187871-A-G
• gnomAD v4: 9-101425589-A-G
• MyVariant Identifiers: chr9:g.104187871A>G (hg19) ; chr9:g.101425589A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101425589A>G , CM000671.2:g.101425589A>G	GRCh38
NC_000009.11:g.104187871A>G , CM000671.1:g.104187871A>G	GRCh37
NC_000009.10:g.103227692A>G	NCBI36
NG_012387.1:g.15192T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.663T>C MANE Select	ENSP00000497767.1:p.His221=
ENST00000648064.1:c.663T>C	ENSP00000497990.1:p.His221=
ENST00000648758.1:c.663T>C	ENSP00000497731.1:p.His221=
ENST00000649902.1:c.663T>C	ENSP00000497216.1:p.His221=
ENST00000374855.8:c.663T>C	ENSP00000363988.4:p.His221=
ENST00000468981.3:n.190T>C
ENST00000616752.1:c.663T>C	ENSP00000481363.1:p.His221=
NM_000035.3:c.663T>C	NP_000026.2:p.His221=
NM_000035.4:c.663T>C MANE Select	NP_000026.2:p.His221=