Canonical Allele Identifier: CA2323505738

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12661354T= , CM000681.2:g.12661354T=	GRCh38
NC_000019.9:g.12772168T= , CM000681.1:g.12772168T=	GRCh37
NC_000019.8:g.12633168T=	NCBI36
NG_008318.1:g.10424A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.932A= MANE Select	ENSP00000395473.2:p.His311=
ENST00000221363.8:c.932A=	ENSP00000221363.4:p.His311=
ENST00000456935.6:c.932A=	ENSP00000395473.2:p.His311=
ENST00000462144.1:n.125A=
ENST00000466794.5:n.914A=
NM_000528.3:c.932A=	NP_000519.2:p.His311=
NM_001173498.1:c.932A=	NP_001166969.1:p.His311=
XM_005259913.1:c.932A=	XP_005259970.1:p.His311=
XM_011528017.1:c.-87A=	XP_011526319.1:n.-87A=
XM_005259913.2:c.932A=	XP_005259970.1:p.His311=
XM_024451518.1:c.-87A=	XP_024307286.1:n.-87A=
NM_000528.4:c.932A= MANE Select	NP_000519.2:p.His311=
NM_001173498.2:c.932A=	NP_001166969.1:p.His311=