Canonical Allele Identifier: CA2323502782

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12655639A= , CM000681.2:g.12655639A=	GRCh38
NC_000019.9:g.12766453A= , CM000681.1:g.12766453A=	GRCh37
NC_000019.8:g.12627453A=	NCBI36
NG_008318.1:g.16139T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1830+55T= MANE Select	ENSP00000395473.2:n.1830+55T=
ENST00000221363.8:c.1827+55T=	ENSP00000221363.4:n.1827+55T=
ENST00000433513.5:n.436+55T=
ENST00000456935.6:c.1830+55T=	ENSP00000395473.2:n.1830+55T=
ENST00000466794.5:n.2420+55T=
ENST00000593686.1:c.423+55T=
ENST00000595880.5:n.427+55T=
ENST00000596591.1:c.194+55T=
NM_000528.3:c.1830+55T=	NP_000519.2:n.1830+55T=
NM_001173498.1:c.1827+55T=	NP_001166969.1:n.1827+55T=
XM_005259913.1:c.1833+55T=	XP_005259970.1:n.1833+55T=
XM_011528017.1:c.729+55T=	XP_011526319.1:n.729+55T=
XM_005259913.2:c.1833+55T=	XP_005259970.1:n.1833+55T=
XM_024451518.1:c.729+55T=	XP_024307286.1:n.729+55T=
NM_000528.4:c.1830+55T= MANE Select	NP_000519.2:n.1830+55T=
NM_001173498.2:c.1827+55T=	NP_001166969.1:n.1827+55T=