Canonical Allele Identifier: CA2323507841

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665709A= , CM000681.2:g.12665709A=	GRCh38
NC_000019.9:g.12776523A= , CM000681.1:g.12776523A=	GRCh37
NC_000019.8:g.12637523A=	NCBI36
NG_008318.1:g.6069T=
NG_015814.1:g.3906A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.256T= MANE Select	ENSP00000395473.2:p.Tyr86=
ENST00000221363.8:c.256T=	ENSP00000221363.4:p.Tyr86=
ENST00000456935.6:c.256T=	ENSP00000395473.2:p.Tyr86=
ENST00000466794.5:n.238T=
ENST00000486847.2:c.160-184T=	ENSP00000470174.1:n.160-184T=
ENST00000596512.5:n.201-184T=
ENST00000597961.1:c.247T=	ENSP00000472710.1:p.Tyr83=
ENST00000598876.1:c.283T=	ENSP00000470533.1:p.Tyr95=
ENST00000600281.1:n.297T=
NM_000528.3:c.256T=	NP_000519.2:p.Tyr86=
NM_001173498.1:c.256T=	NP_001166969.1:p.Tyr86=
XM_005259913.1:c.256T=	XP_005259970.1:p.Tyr86=
XM_005259913.2:c.256T=	XP_005259970.1:p.Tyr86=
XM_024451518.1:c.-763T=	XP_024307286.1:n.-763T=
NM_000528.4:c.256T= MANE Select	NP_000519.2:p.Tyr86=
NM_001173498.2:c.256T=	NP_001166969.1:p.Tyr86=