Canonical Allele Identifier: CA2323507605

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665220G= , CM000681.2:g.12665220G=	GRCh38
NC_000019.9:g.12776034G= , CM000681.1:g.12776034G=	GRCh37
NC_000019.8:g.12637034G=	NCBI36
NG_008318.1:g.6558C=
NG_015814.1:g.3417G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.436+132C= MANE Select	ENSP00000395473.2:n.436+132C=
ENST00000221363.8:c.436+132C=	ENSP00000221363.4:n.436+132C=
ENST00000456935.6:c.436+132C=	ENSP00000395473.2:n.436+132C=
ENST00000466794.5:n.418+132C=
ENST00000486847.2:c.333+132C=	ENSP00000470174.1:n.333+132C=
ENST00000596512.5:n.374+132C=
ENST00000597961.1:c.427+132C=	ENSP00000472710.1:n.427+132C=
ENST00000598876.1:c.463+132C=	ENSP00000470533.1:n.463+132C=
NM_000528.3:c.436+132C=	NP_000519.2:n.436+132C=
NM_001173498.1:c.436+132C=	NP_001166969.1:n.436+132C=
XM_005259913.1:c.436+132C=	XP_005259970.1:n.436+132C=
XM_005259913.2:c.436+132C=	XP_005259970.1:n.436+132C=
XM_024451518.1:c.-583+132C=	XP_024307286.1:n.-583+132C=
NM_000528.4:c.436+132C= MANE Select	NP_000519.2:n.436+132C=
NM_001173498.2:c.436+132C=	NP_001166969.1:n.436+132C=