Canonical Allele Identifier: CA1868279632

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101426590G= , CM000671.2:g.101426590G=	GRCh38
NC_000009.11:g.104188872G= , CM000671.1:g.104188872G=	GRCh37
NC_000009.10:g.103228693G=	NCBI36
NG_012387.1:g.14191C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.589C= MANE Select	ENSP00000497767.1:p.His197=
ENST00000648064.1:c.589C=	ENSP00000497990.1:p.His197=
ENST00000648758.1:c.589C=	ENSP00000497731.1:p.His197=
ENST00000649902.1:c.589C=	ENSP00000497216.1:p.His197=
ENST00000374855.8:c.589C=	ENSP00000363988.4:p.His197=
ENST00000468981.3:n.116C=
ENST00000616752.1:c.589C=	ENSP00000481363.1:p.His197=
NM_000035.3:c.589C=	NP_000026.2:p.His197=
NM_000035.4:c.589C= MANE Select	NP_000026.2:p.His197=