Canonical Allele Identifier: CA2323503480

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657024T= , CM000681.2:g.12657024T=	GRCh38
NC_000019.9:g.12767838T= , CM000681.1:g.12767838T=	GRCh37
NC_000019.8:g.12628838T=	NCBI36
NG_008318.1:g.14754A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1452A= MANE Select	ENSP00000395473.2:p.Arg484=
ENST00000221363.8:c.1449A=	ENSP00000221363.4:p.Arg483=
ENST00000433513.5:n.58A=
ENST00000456935.6:c.1452A=	ENSP00000395473.2:p.Arg484=
ENST00000466794.5:n.1351A=
ENST00000495617.1:n.628A=
ENST00000593686.1:c.62A=
ENST00000595880.5:n.49A=
NM_000528.3:c.1452A=	NP_000519.2:p.Arg484=
NM_001173498.1:c.1449A=	NP_001166969.1:p.Arg483=
XM_005259913.1:c.1455A=	XP_005259970.1:p.Arg485=
XM_011528017.1:c.351A=	XP_011526319.1:p.Arg117=
XM_005259913.2:c.1455A=	XP_005259970.1:p.Arg485=
XM_024451518.1:c.351A=	XP_024307286.1:p.Arg117=
NM_000528.4:c.1452A= MANE Select	NP_000519.2:p.Arg484=
NM_001173498.2:c.1449A=	NP_001166969.1:p.Arg483=