Canonical Allele Identifier: CA2323498566

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647297C= , CM000681.2:g.12647297C=	GRCh38
NC_000019.9:g.12758111C= , CM000681.1:g.12758111C=	GRCh37
NC_000019.8:g.12619111C=	NCBI36
NG_008318.1:g.24481G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2859G= MANE Select	ENSP00000395473.2:p.Glu953=
ENST00000221363.8:c.2856G=	ENSP00000221363.4:p.Glu952=
ENST00000456935.6:c.2859G=	ENSP00000395473.2:p.Glu953=
ENST00000466794.5:n.3449G=
ENST00000469423.1:n.288G=
ENST00000493218.5:n.270G=
ENST00000597692.1:c.418G=
NM_000528.3:c.2859G=	NP_000519.2:p.Glu953=
NM_001173498.1:c.2856G=	NP_001166969.1:p.Glu952=
XM_005259913.1:c.2862G=	XP_005259970.1:p.Glu954=
XM_011528017.1:c.1758G=	XP_011526319.1:p.Glu586=
XM_005259913.2:c.2862G=	XP_005259970.1:p.Glu954=
XM_024451518.1:c.1758G=	XP_024307286.1:p.Glu586=
NM_000528.4:c.2859G= MANE Select	NP_000519.2:p.Glu953=
NM_001173498.2:c.2856G=	NP_001166969.1:p.Glu952=