Canonical Allele Identifier: CA2323507875

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665789T= , CM000681.2:g.12665789T=	GRCh38
NC_000019.9:g.12776603T= , CM000681.1:g.12776603T=	GRCh37
NC_000019.8:g.12637603T=	NCBI36
NG_008318.1:g.5989A=
NG_015814.1:g.3986T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.176A= MANE Select	ENSP00000395473.2:p.Gln59=
ENST00000221363.8:c.176A=	ENSP00000221363.4:p.Gln59=
ENST00000456935.6:c.176A=	ENSP00000395473.2:p.Gln59=
ENST00000466794.5:n.158A=
ENST00000486847.2:c.160-264A=	ENSP00000470174.1:n.160-264A=
ENST00000596512.5:n.201-264A=
ENST00000597961.1:c.167A=	ENSP00000472710.1:p.Gln56=
ENST00000598876.1:c.203A=	ENSP00000470533.1:p.Gln68=
ENST00000600281.1:n.217A=
NM_000528.3:c.176A=	NP_000519.2:p.Gln59=
NM_001173498.1:c.176A=	NP_001166969.1:p.Gln59=
XM_005259913.1:c.176A=	XP_005259970.1:p.Gln59=
XM_005259913.2:c.176A=	XP_005259970.1:p.Gln59=
XM_024451518.1:c.-843A=	XP_024307286.1:n.-843A=
NM_000528.4:c.176A= MANE Select	NP_000519.2:p.Gln59=
NM_001173498.2:c.176A=	NP_001166969.1:p.Gln59=