Canonical Allele Identifier: CA1140222244

Gene: FCGR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161671427C= , CM000663.2:g.161671427C=	GRCh38
NC_000001.10:g.161641217C= , CM000663.1:g.161641217C=	GRCh37
NC_000001.9:g.159907841C=	NCBI36
NG_023318.1:g.13313C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.169C= MANE Select	ENSP00000351497.5:p.Gln57=
ENST00000674150.1:n.261C=
ENST00000236937.13:c.169C=	ENSP00000236937.9:p.Gln57=
ENST00000358671.9:c.169C=	ENSP00000351497.5:p.Gln57=
ENST00000367961.8:c.148C=	ENSP00000356938.4:p.Gln50=
ENST00000428605.3:c.169C=	ENSP00000404329.3:p.Gln57=
ENST00000480308.5:n.219C=
ENST00000485778.1:n.212C=
NM_001002273.2:c.166C=	NP_001002273.1:p.Gln56=
NM_001002274.2:c.169C=	NP_001002274.1:p.Gln57=
NM_001002275.2:c.166C=	NP_001002275.1:p.Gln56=
NM_001190828.1:c.148C=	NP_001177757.1:p.Gln50=
NM_004001.4:c.169C=	NP_003992.3:p.Gln57=
XM_011509292.1:c.169C=	XP_011507594.1:p.Gln57=
XM_017000670.2:c.166C=	XP_016856159.1:p.Gln56=
XM_024454043.1:c.169C=	XP_024309811.1:p.Gln57=
XM_024454044.1:c.166C=	XP_024309812.1:p.Gln56=
XM_024454045.1:c.166C=	XP_024309813.1:p.Gln56=
XM_024454047.1:c.169C=	XP_024309815.1:p.Gln57=
XR_002959731.1:n.260C=
NM_001002273.3:c.166C=	NP_001002273.1:p.Gln56=
NM_001002274.3:c.169C=	NP_001002274.1:p.Gln57=
NM_001002275.3:c.166C=	NP_001002275.1:p.Gln56=
NM_001190828.2:c.148C=	NP_001177757.1:p.Gln50=
NM_001386000.1:c.145C=	NP_001372929.1:p.Gln49=
NM_001386001.1:c.148C=	NP_001372930.1:p.Gln50=
NM_001386002.1:c.145C=	NP_001372931.1:p.Gln49=
NM_001386003.1:c.169C=	NP_001372932.1:p.Gln57=
NM_001386004.1:c.145C=	NP_001372933.1:p.Gln49=
NM_001386005.1:c.169C=	NP_001372934.1:p.Gln57=
NM_001386006.1:c.148C=	NP_001372935.1:p.Gln50=
NM_004001.5:c.169C=	NP_003992.3:p.Gln57=
NR_169827.1:n.260C=
NM_001394477.1:c.169C= MANE Select	NP_001381406.1:p.Gln57=