Canonical Allele Identifier: CA2323507679

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665369C= , CM000681.2:g.12665369C=	GRCh38
NC_000019.9:g.12776183C= , CM000681.1:g.12776183C=	GRCh37
NC_000019.8:g.12637183C=	NCBI36
NG_008318.1:g.6409G=
NG_015814.1:g.3566C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.419G= MANE Select	ENSP00000395473.2:p.Arg140=
ENST00000221363.8:c.419G=	ENSP00000221363.4:p.Arg140=
ENST00000456935.6:c.419G=	ENSP00000395473.2:p.Arg140=
ENST00000466794.5:n.401G=
ENST00000486847.2:c.316G=	ENSP00000470174.1:p.Glu106=
ENST00000596512.5:n.357G=
ENST00000597961.1:c.410G=	ENSP00000472710.1:p.Arg137=
ENST00000598876.1:c.446G=	ENSP00000470533.1:p.Arg149=
ENST00000600281.1:n.460G=
NM_000528.3:c.419G=	NP_000519.2:p.Arg140=
NM_001173498.1:c.419G=	NP_001166969.1:p.Arg140=
XM_005259913.1:c.419G=	XP_005259970.1:p.Arg140=
XM_005259913.2:c.419G=	XP_005259970.1:p.Arg140=
XM_024451518.1:c.-600G=	XP_024307286.1:n.-600G=
NM_000528.4:c.419G= MANE Select	NP_000519.2:p.Arg140=
NM_001173498.2:c.419G=	NP_001166969.1:p.Arg140=