Canonical Allele Identifier: CA2323507669

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665352C= , CM000681.2:g.12665352C=	GRCh38
NC_000019.9:g.12776166C= , CM000681.1:g.12776166C=	GRCh37
NC_000019.8:g.12637166C=	NCBI36
NG_008318.1:g.6426G=
NG_015814.1:g.3549C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.436G= MANE Select	ENSP00000395473.2:p.Gly146=
ENST00000221363.8:c.436G=	ENSP00000221363.4:p.Gly146=
ENST00000456935.6:c.436G=	ENSP00000395473.2:p.Gly146=
ENST00000466794.5:n.418G=
ENST00000486847.2:c.333G=	ENSP00000470174.1:p.Arg111=
ENST00000596512.5:n.374G=
ENST00000597961.1:c.427G=	ENSP00000472710.1:p.Gly143=
ENST00000598876.1:c.463G=	ENSP00000470533.1:p.Gly155=
ENST00000600281.1:n.477G=
NM_000528.3:c.436G=	NP_000519.2:p.Gly146=
NM_001173498.1:c.436G=	NP_001166969.1:p.Gly146=
XM_005259913.1:c.436G=	XP_005259970.1:p.Gly146=
XM_005259913.2:c.436G=	XP_005259970.1:p.Gly146=
XM_024451518.1:c.-583G=	XP_024307286.1:n.-583G=
NM_000528.4:c.436G= MANE Select	NP_000519.2:p.Gly146=
NM_001173498.2:c.436G=	NP_001166969.1:p.Gly146=