Canonical Allele Identifier: CA1140055029

Gene: FCGR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161629864G= , CM000663.2:g.161629864G=	GRCh38
NC_000001.10:g.161599654G= , CM000663.1:g.161599654G=	GRCh37
NC_000001.9:g.159866278G=	NCBI36
NG_032926.1:g.7100C=
NG_032926.2:g.7100C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421702.4:c.230C=	ENSP00000394204.3:p.Ala77=
ENST00000533780.2:n.609C=
ENST00000699402.1:c.40+1191C=	ENSP00000514363.1:n.40+1191C=
ENST00000699403.1:c.61+504C=	ENSP00000514364.1:n.61+504C=
ENST00000699523.1:n.150C=
ENST00000421702.3:c.230C=	ENSP00000394204.3:p.Ala77=
ENST00000650385.1:c.233C= MANE Select	ENSP00000497461.1:p.Ala78=
ENST00000294800.7:c.233C=	ENSP00000294800.3:p.Ala78=
ENST00000367964.6:c.233C=	ENSP00000356941.2:p.Ala78=
ENST00000421702.2:c.294C=
ENST00000531221.5:c.341C=	ENSP00000433642.1:p.Ala114=
ENST00000533780.1:n.387C=
ENST00000534776.1:c.182C=	ENSP00000437084.1:p.Ala61=
ENST00000613418.4:c.182C=	ENSP00000482838.1:p.Ala61=
ENST00000614870.4:c.182C=	ENSP00000478466.1:p.Ala61=
NM_000570.4:c.233C=	NP_000561.3:p.Ala78=
NM_001244753.1:c.341C=	NP_001231682.1:p.Ala114=
NM_001271035.1:c.338C=	NP_001257964.1:p.Ala113=
NM_001271036.1:c.182C=	NP_001257965.1:p.Ala61=
NM_001271037.1:c.182C=	NP_001257966.1:p.Ala61=
NM_001244753.2:c.233C= MANE Select	NP_001231682.2:p.Ala78=
NM_001271035.2:c.230C=	NP_001257964.2:p.Ala77=
NM_000570.5:c.233C=	NP_000561.3:p.Ala78=
NM_001271036.2:c.182C=	NP_001257965.1:p.Ala61=
NM_001271037.2:c.182C=	NP_001257966.1:p.Ala61=