Canonical Allele Identifier: CA857735145

Gene: ALDOB

Linked Data

• dbSNP Id: rs1236790832
• MyVariant Identifiers: chr9:g.104192317A>G (hg19) ; chr9:g.101430035A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430035A>G , CM000671.2:g.101430035A>G	GRCh38
NC_000009.11:g.104192317A>G , CM000671.1:g.104192317A>G	GRCh37
NC_000009.10:g.103232138A>G	NCBI36
NG_012387.1:g.10746T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.113-69T>C MANE Select	ENSP00000497767.1:n.113-69T>C
ENST00000648064.1:c.113-69T>C	ENSP00000497990.1:n.113-69T>C
ENST00000648423.1:c.113-69T>C	ENSP00000497985.1:n.113-69T>C
ENST00000648758.1:c.113-69T>C	ENSP00000497731.1:n.113-69T>C
ENST00000648906.1:n.283-69T>C
ENST00000649902.1:c.113-69T>C	ENSP00000497216.1:n.113-69T>C
ENST00000650613.1:n.189-69T>C
ENST00000374855.8:c.113-69T>C	ENSP00000363988.4:n.113-69T>C
ENST00000616752.1:c.113-69T>C	ENSP00000481363.1:n.113-69T>C
NM_000035.3:c.113-69T>C	NP_000026.2:n.113-69T>C
NM_000035.4:c.113-69T>C MANE Select	NP_000026.2:n.113-69T>C