Canonical Allele Identifier: CA2323499574

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12649189T= , CM000681.2:g.12649189T=	GRCh38
NC_000019.9:g.12760003T= , CM000681.1:g.12760003T=	GRCh37
NC_000019.8:g.12621003T=	NCBI36
NG_008318.1:g.22589A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2383A= MANE Select	ENSP00000395473.2:p.Thr795=
ENST00000221363.8:c.2380A=	ENSP00000221363.4:p.Thr794=
ENST00000456935.6:c.2383A=	ENSP00000395473.2:p.Thr795=
ENST00000466794.5:n.2973A=
NM_000528.3:c.2383A=	NP_000519.2:p.Thr795=
NM_001173498.1:c.2380A=	NP_001166969.1:p.Thr794=
XM_005259913.1:c.2386A=	XP_005259970.1:p.Thr796=
XM_011528017.1:c.1282A=	XP_011526319.1:p.Thr428=
XM_005259913.2:c.2386A=	XP_005259970.1:p.Thr796=
XM_024451518.1:c.1282A=	XP_024307286.1:p.Thr428=
NM_000528.4:c.2383A= MANE Select	NP_000519.2:p.Thr795=
NM_001173498.2:c.2380A=	NP_001166969.1:p.Thr794=