Canonical Allele Identifier: CA466463108

Gene: ALDOB

Linked Data

• MyVariant Identifiers: chr9:g.104193059T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101430777T>G , CM000671.2:g.101430777T>G	GRCh38
NC_000009.11:g.104193059T>G , CM000671.1:g.104193059T>G	GRCh37
NC_000009.10:g.103232880T>G	NCBI36
NG_012387.1:g.10004A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.111A>C MANE Select	ENSP00000497767.1:p.Val37=
ENST00000648064.1:c.111A>C	ENSP00000497990.1:p.Val37=
ENST00000648423.1:c.111A>C	ENSP00000497985.1:p.Val37=
ENST00000648758.1:c.111A>C	ENSP00000497731.1:p.Val37=
ENST00000648906.1:n.281A>C
ENST00000649902.1:c.111A>C	ENSP00000497216.1:p.Val37=
ENST00000650613.1:n.187A>C
ENST00000374855.8:c.111A>C	ENSP00000363988.4:p.Val37=
ENST00000616752.1:c.111A>C	ENSP00000481363.1:p.Val37=
NM_000035.3:c.111A>C	NP_000026.2:p.Val37=
NM_000035.4:c.111A>C MANE Select	NP_000026.2:p.Val37=