Canonical Allele Identifier: CA2323507394

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12664793T= , CM000681.2:g.12664793T=	GRCh38
NC_000019.9:g.12775607T= , CM000681.1:g.12775607T=	GRCh37
NC_000019.8:g.12636607T=	NCBI36
NG_008318.1:g.6985A=
NG_015814.1:g.2990T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.629A= MANE Select	ENSP00000395473.2:p.Gln210=
ENST00000221363.8:c.629A=	ENSP00000221363.4:p.Gln210=
ENST00000456935.6:c.629A=	ENSP00000395473.2:p.Gln210=
ENST00000466794.5:n.611A=
ENST00000486847.2:c.333+559A=	ENSP00000470174.1:n.333+559A=
NM_000528.3:c.629A=	NP_000519.2:p.Gln210=
NM_001173498.1:c.629A=	NP_001166969.1:p.Gln210=
XM_005259913.1:c.629A=	XP_005259970.1:p.Gln210=
XM_005259913.2:c.629A=	XP_005259970.1:p.Gln210=
XM_024451518.1:c.-390A=	XP_024307286.1:n.-390A=
NM_000528.4:c.629A= MANE Select	NP_000519.2:p.Gln210=
NM_001173498.2:c.629A=	NP_001166969.1:p.Gln210=