Canonical Allele Identifier: CA1868275298

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421553G= , CM000671.2:g.101421553G=	GRCh38
NC_000009.11:g.104183835G= , CM000671.1:g.104183835G=	GRCh37
NC_000009.10:g.103223656G=	NCBI36
NG_012387.1:g.19228C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647789.2:c.*256C= MANE Select	ENSP00000497767.1:n.*256C=
ENST00000648064.1:c.*256C=	ENSP00000497990.1:n.*256C=
ENST00000374855.8:c.*256C=	ENSP00000363988.4:n.*256C=
ENST00000616752.1:c.*363C=	ENSP00000481363.1:n.*363C=
NM_000035.3:c.*256C=	NP_000026.2:n.*256C=
NM_000035.4:c.*256C= MANE Select	NP_000026.2:n.*256C=