Canonical Allele Identifier: CA1202839755

Gene: FCGR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161674003T= , CM000663.2:g.161674003T=	GRCh38
NC_000001.10:g.161643793T= , CM000663.1:g.161643793T=	GRCh37
NC_000001.9:g.159910417T=	NCBI36
NG_023318.1:g.15889T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.690T= MANE Select	ENSP00000351497.5:p.Thr230=
ENST00000236937.13:c.690T=	ENSP00000236937.9:p.Thr230=
ENST00000358671.9:c.690T=	ENSP00000351497.5:p.Thr230=
ENST00000367961.8:c.669T=	ENSP00000356938.4:p.Thr223=
ENST00000428605.3:c.690T=	ENSP00000404329.3:p.Thr230=
ENST00000480308.5:n.740T=
ENST00000485778.1:n.2058T=
NM_001002273.2:c.687T=	NP_001002273.1:p.Thr229=
NM_001002274.2:c.690T=	NP_001002274.1:p.Thr230=
NM_001002275.2:c.687T=	NP_001002275.1:p.Thr229=
NM_001190828.1:c.669T=	NP_001177757.1:p.Thr223=
NM_004001.4:c.690T=	NP_003992.3:p.Thr230=
XM_017000670.2:c.687T=	XP_016856159.1:p.Thr229=
XM_024454043.1:c.690T=	XP_024309811.1:p.Thr230=
XM_024454044.1:c.687T=	XP_024309812.1:p.Thr229=
XM_024454045.1:c.687T=	XP_024309813.1:p.Thr229=
NM_001002273.3:c.687T=	NP_001002273.1:p.Thr229=
NM_001002274.3:c.690T=	NP_001002274.1:p.Thr230=
NM_001002275.3:c.687T=	NP_001002275.1:p.Thr229=
NM_001190828.2:c.669T=	NP_001177757.1:p.Thr223=
NM_001386000.1:c.666T=	NP_001372929.1:p.Thr222=
NM_001386001.1:c.669T=	NP_001372930.1:p.Thr223=
NM_001386002.1:c.666T=	NP_001372931.1:p.Thr222=
NM_001386003.1:c.690T=	NP_001372932.1:p.Thr230=
NM_001386004.1:c.666T=	NP_001372933.1:p.Thr222=
NM_001386005.1:c.690T=	NP_001372934.1:p.Thr230=
NM_001386006.1:c.669T=	NP_001372935.1:p.Thr223=
NM_004001.5:c.690T=	NP_003992.3:p.Thr230=
NR_169827.1:n.919T=
NM_001394477.1:c.690T= MANE Select	NP_001381406.1:p.Thr230=