Canonical Allele Identifier: CA2323506880

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12663717G= , CM000681.2:g.12663717G=	GRCh38
NC_000019.9:g.12774531G= , CM000681.1:g.12774531G=	GRCh37
NC_000019.8:g.12635531G=	NCBI36
NG_008318.1:g.8061C=
NG_015814.1:g.1914G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.749C= MANE Select	ENSP00000395473.2:p.Ala250=
ENST00000221363.8:c.749C=	ENSP00000221363.4:p.Ala250=
ENST00000456935.6:c.749C=	ENSP00000395473.2:p.Ala250=
ENST00000466794.5:n.731C=
ENST00000486847.2:c.452C=	ENSP00000470174.1:p.Ala151=
NM_000528.3:c.749C=	NP_000519.2:p.Ala250=
NM_001173498.1:c.749C=	NP_001166969.1:p.Ala250=
XM_005259913.1:c.749C=	XP_005259970.1:p.Ala250=
XM_005259913.2:c.749C=	XP_005259970.1:p.Ala250=
XM_024451518.1:c.-270C=	XP_024307286.1:n.-270C=
NM_000528.4:c.749C= MANE Select	NP_000519.2:p.Ala250=
NM_001173498.2:c.749C=	NP_001166969.1:p.Ala250=