Canonical Allele Identifier: CA2323499643

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12649341C= , CM000681.2:g.12649341C=	GRCh38
NC_000019.9:g.12760155C= , CM000681.1:g.12760155C=	GRCh37
NC_000019.8:g.12621155C=	NCBI36
NG_008318.1:g.22437G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2355G= MANE Select	ENSP00000395473.2:p.Thr785=
ENST00000221363.8:c.2352G=	ENSP00000221363.4:p.Thr784=
ENST00000456935.6:c.2355G=	ENSP00000395473.2:p.Thr785=
ENST00000466794.5:n.2945G=
NM_000528.3:c.2355G=	NP_000519.2:p.Thr785=
NM_001173498.1:c.2352G=	NP_001166969.1:p.Thr784=
XM_005259913.1:c.2358G=	XP_005259970.1:p.Thr786=
XM_011528017.1:c.1254G=	XP_011526319.1:p.Thr418=
XM_005259913.2:c.2358G=	XP_005259970.1:p.Thr786=
XM_024451518.1:c.1254G=	XP_024307286.1:p.Thr418=
NM_000528.4:c.2355G= MANE Select	NP_000519.2:p.Thr785=
NM_001173498.2:c.2352G=	NP_001166969.1:p.Thr784=