Canonical Allele Identifier: CA2323507878

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665800G= , CM000681.2:g.12665800G=	GRCh38
NC_000019.9:g.12776614G= , CM000681.1:g.12776614G=	GRCh37
NC_000019.8:g.12637614G=	NCBI36
NG_008318.1:g.5978C=
NG_015814.1:g.3997G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.165C= MANE Select	ENSP00000395473.2:p.Cys55=
ENST00000221363.8:c.165C=	ENSP00000221363.4:p.Cys55=
ENST00000456935.6:c.165C=	ENSP00000395473.2:p.Cys55=
ENST00000466794.5:n.147C=
ENST00000486847.2:c.160-275C=	ENSP00000470174.1:n.160-275C=
ENST00000596512.5:n.201-275C=
ENST00000597961.1:c.156C=	ENSP00000472710.1:p.Cys52=
ENST00000598876.1:c.192C=	ENSP00000470533.1:p.Cys64=
ENST00000600281.1:n.206C=
NM_000528.3:c.165C=	NP_000519.2:p.Cys55=
NM_001173498.1:c.165C=	NP_001166969.1:p.Cys55=
XM_005259913.1:c.165C=	XP_005259970.1:p.Cys55=
XM_005259913.2:c.165C=	XP_005259970.1:p.Cys55=
XM_024451518.1:c.-854C=	XP_024307286.1:n.-854C=
NM_000528.4:c.165C= MANE Select	NP_000519.2:p.Cys55=
NM_001173498.2:c.165C=	NP_001166969.1:p.Cys55=