Canonical Allele Identifier: CA2323506911

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12663807C= , CM000681.2:g.12663807C=	GRCh38
NC_000019.9:g.12774621C= , CM000681.1:g.12774621C=	GRCh37
NC_000019.8:g.12635621C=	NCBI36
NG_008318.1:g.7971G=
NG_015814.1:g.2004C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.659G= MANE Select	ENSP00000395473.2:p.Arg220=
ENST00000221363.8:c.659G=	ENSP00000221363.4:p.Arg220=
ENST00000456935.6:c.659G=	ENSP00000395473.2:p.Arg220=
ENST00000466794.5:n.641G=
ENST00000486847.2:c.362G=	ENSP00000470174.1:p.Arg121=
NM_000528.3:c.659G=	NP_000519.2:p.Arg220=
NM_001173498.1:c.659G=	NP_001166969.1:p.Arg220=
XM_005259913.1:c.659G=	XP_005259970.1:p.Arg220=
XM_005259913.2:c.659G=	XP_005259970.1:p.Arg220=
XM_024451518.1:c.-360G=	XP_024307286.1:n.-360G=
NM_000528.4:c.659G= MANE Select	NP_000519.2:p.Arg220=
NM_001173498.2:c.659G=	NP_001166969.1:p.Arg220=