Canonical Allele Identifier: CA2323498663

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647492C= , CM000681.2:g.12647492C=	GRCh38
NC_000019.9:g.12758306C= , CM000681.1:g.12758306C=	GRCh37
NC_000019.8:g.12619306C=	NCBI36
NG_008318.1:g.24286G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2771G= MANE Select	ENSP00000395473.2:p.Gly924=
ENST00000221363.8:c.2768G=	ENSP00000221363.4:p.Gly923=
ENST00000456935.6:c.2771G=	ENSP00000395473.2:p.Gly924=
ENST00000466794.5:n.3361G=
ENST00000469423.1:n.93G=
ENST00000493218.5:n.182G=
ENST00000597692.1:c.330G=
NM_000528.3:c.2771G=	NP_000519.2:p.Gly924=
NM_001173498.1:c.2768G=	NP_001166969.1:p.Gly923=
XM_005259913.1:c.2774G=	XP_005259970.1:p.Gly925=
XM_011528017.1:c.1670G=	XP_011526319.1:p.Gly557=
XM_005259913.2:c.2774G=	XP_005259970.1:p.Gly925=
XM_024451518.1:c.1670G=	XP_024307286.1:p.Gly557=
NM_000528.4:c.2771G= MANE Select	NP_000519.2:p.Gly924=
NM_001173498.2:c.2768G=	NP_001166969.1:p.Gly923=