Canonical Allele Identifier: CA2323507886

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665822A= , CM000681.2:g.12665822A=	GRCh38
NC_000019.9:g.12776636A= , CM000681.1:g.12776636A=	GRCh37
NC_000019.8:g.12637636A=	NCBI36
NG_008318.1:g.5956T=
NG_015814.1:g.4019A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.160-17T= MANE Select	ENSP00000395473.2:n.160-17T=
ENST00000221363.8:c.160-17T=	ENSP00000221363.4:n.160-17T=
ENST00000456935.6:c.160-17T=	ENSP00000395473.2:n.160-17T=
ENST00000466794.5:n.142-17T=
ENST00000486847.2:c.160-297T=	ENSP00000470174.1:n.160-297T=
ENST00000596512.5:n.201-297T=
ENST00000597961.1:c.151-17T=	ENSP00000472710.1:n.151-17T=
ENST00000598876.1:c.170T=	ENSP00000470533.1:p.Phe57=
ENST00000600281.1:n.201-17T=
NM_000528.3:c.160-17T=	NP_000519.2:n.160-17T=
NM_001173498.1:c.160-17T=	NP_001166969.1:n.160-17T=
XM_005259913.1:c.160-17T=	XP_005259970.1:n.160-17T=
XM_005259913.2:c.160-17T=	XP_005259970.1:n.160-17T=
XM_024451518.1:c.-859-17T=	XP_024307286.1:n.-859-17T=
NM_000528.4:c.160-17T= MANE Select	NP_000519.2:n.160-17T=
NM_001173498.2:c.160-17T=	NP_001166969.1:n.160-17T=