Canonical Allele Identifier: CA2323499596

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12649248T= , CM000681.2:g.12649248T=	GRCh38
NC_000019.9:g.12760062T= , CM000681.1:g.12760062T=	GRCh37
NC_000019.8:g.12621062T=	NCBI36
NG_008318.1:g.22530A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2356-32A= MANE Select	ENSP00000395473.2:n.2356-32A=
ENST00000221363.8:c.2353-32A=	ENSP00000221363.4:n.2353-32A=
ENST00000456935.6:c.2356-32A=	ENSP00000395473.2:n.2356-32A=
ENST00000466794.5:n.2946-32A=
NM_000528.3:c.2356-32A=	NP_000519.2:n.2356-32A=
NM_001173498.1:c.2353-32A=	NP_001166969.1:n.2353-32A=
XM_005259913.1:c.2359-32A=	XP_005259970.1:n.2359-32A=
XM_011528017.1:c.1255-32A=	XP_011526319.1:n.1255-32A=
XM_005259913.2:c.2359-32A=	XP_005259970.1:n.2359-32A=
XM_024451518.1:c.1255-32A=	XP_024307286.1:n.1255-32A=
NM_000528.4:c.2356-32A= MANE Select	NP_000519.2:n.2356-32A=
NM_001173498.2:c.2353-32A=	NP_001166969.1:n.2353-32A=