Canonical Allele Identifier: CA2323506906

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12663788C= , CM000681.2:g.12663788C=	GRCh38
NC_000019.9:g.12774602C= , CM000681.1:g.12774602C=	GRCh37
NC_000019.8:g.12635602C=	NCBI36
NG_008318.1:g.7990G=
NG_015814.1:g.1985C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.678G= MANE Select	ENSP00000395473.2:p.Lys226=
ENST00000221363.8:c.678G=	ENSP00000221363.4:p.Lys226=
ENST00000456935.6:c.678G=	ENSP00000395473.2:p.Lys226=
ENST00000466794.5:n.660G=
ENST00000486847.2:c.381G=	ENSP00000470174.1:p.Lys127=
NM_000528.3:c.678G=	NP_000519.2:p.Lys226=
NM_001173498.1:c.678G=	NP_001166969.1:p.Lys226=
XM_005259913.1:c.678G=	XP_005259970.1:p.Lys226=
XM_005259913.2:c.678G=	XP_005259970.1:p.Lys226=
XM_024451518.1:c.-341G=	XP_024307286.1:n.-341G=
NM_000528.4:c.678G= MANE Select	NP_000519.2:p.Lys226=
NM_001173498.2:c.678G=	NP_001166969.1:p.Lys226=