Canonical Allele Identifier: CA2323503431

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12656921T= , CM000681.2:g.12656921T=	GRCh38
NC_000019.9:g.12767735T= , CM000681.1:g.12767735T=	GRCh37
NC_000019.8:g.12628735T=	NCBI36
NG_008318.1:g.14857A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1527+28A= MANE Select	ENSP00000395473.2:n.1527+28A=
ENST00000221363.8:c.1524+28A=	ENSP00000221363.4:n.1524+28A=
ENST00000433513.5:n.133+28A=
ENST00000456935.6:c.1527+28A=	ENSP00000395473.2:n.1527+28A=
ENST00000466794.5:n.1426+28A=
ENST00000495617.1:n.703+28A=
ENST00000593686.1:c.137+28A=
ENST00000595880.5:n.124+28A=
NM_000528.3:c.1527+28A=	NP_000519.2:n.1527+28A=
NM_001173498.1:c.1524+28A=	NP_001166969.1:n.1524+28A=
XM_005259913.1:c.1530+28A=	XP_005259970.1:n.1530+28A=
XM_011528017.1:c.426+28A=	XP_011526319.1:n.426+28A=
XM_005259913.2:c.1530+28A=	XP_005259970.1:n.1530+28A=
XM_024451518.1:c.426+28A=	XP_024307286.1:n.426+28A=
NM_000528.4:c.1527+28A= MANE Select	NP_000519.2:n.1527+28A=
NM_001173498.2:c.1524+28A=	NP_001166969.1:n.1524+28A=