Canonical Allele Identifier: CA1202839531

Gene: FCGR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161673499_161673500delinsCT , CM000663.2:g.161673499_161673500delinsCT	GRCh38
NC_000001.10:g.161643289_161643290delinsCT , CM000663.1:g.161643289_161643290delinsCT	GRCh37
NC_000001.9:g.159909913_159909914delinsCT	NCBI36
NG_023318.1:g.15385_15386delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.646+270_646+271delinsCT MANE Select	ENSP00000351497.5:n.646+270_646+271delinsCT
ENST00000236937.13:c.646+270_646+271delinsCT	ENSP00000236937.9:n.646+270_646+271delinsCT
ENST00000358671.9:c.646+270_646+271delinsCT	ENSP00000351497.5:n.646+270_646+271delinsCT
ENST00000367961.8:c.625+270_625+271delinsCT	ENSP00000356938.4:n.625+270_625+271delinsCT
ENST00000428605.3:c.646+270_646+271delinsCT	ENSP00000404329.3:n.646+270_646+271delinsCT
ENST00000480308.5:n.696+270_696+271delinsCT
ENST00000485778.1:n.2014+270_2014+271delinsCT
NM_001002273.2:c.643+270_643+271delinsCT	NP_001002273.1:n.643+270_643+271delinsCT
NM_001002274.2:c.646+270_646+271delinsCT	NP_001002274.1:n.646+270_646+271delinsCT
NM_001002275.2:c.643+270_643+271delinsCT	NP_001002275.1:n.643+270_643+271delinsCT
NM_001190828.1:c.625+270_625+271delinsCT	NP_001177757.1:n.625+270_625+271delinsCT
NM_004001.4:c.646+270_646+271delinsCT	NP_003992.3:n.646+270_646+271delinsCT
XM_011509292.1:c.682_683delinsCT	XP_011507594.1:p.Leu228=
XM_017000670.2:c.643+270_643+271delinsCT	XP_016856159.1:n.643+270_643+271delinsCT
XM_024454043.1:c.646+270_646+271delinsCT	XP_024309811.1:n.646+270_646+271delinsCT
XM_024454044.1:c.643+270_643+271delinsCT	XP_024309812.1:n.643+270_643+271delinsCT
XM_024454045.1:c.643+270_643+271delinsCT	XP_024309813.1:n.643+270_643+271delinsCT
XM_024454047.1:c.682_683delinsCT	XP_024309815.1:p.Leu228=
NM_001002273.3:c.643+270_643+271delinsCT	NP_001002273.1:n.643+270_643+271delinsCT
NM_001002274.3:c.646+270_646+271delinsCT	NP_001002274.1:n.646+270_646+271delinsCT
NM_001002275.3:c.643+270_643+271delinsCT	NP_001002275.1:n.643+270_643+271delinsCT
NM_001190828.2:c.625+270_625+271delinsCT	NP_001177757.1:n.625+270_625+271delinsCT
NM_001386000.1:c.622+270_622+271delinsCT	NP_001372929.1:n.622+270_622+271delinsCT
NM_001386001.1:c.625+270_625+271delinsCT	NP_001372930.1:n.625+270_625+271delinsCT
NM_001386002.1:c.622+270_622+271delinsCT	NP_001372931.1:n.622+270_622+271delinsCT
NM_001386003.1:c.646+270_646+271delinsCT	NP_001372932.1:n.646+270_646+271delinsCT
NM_001386004.1:c.622+270_622+271delinsCT	NP_001372933.1:n.622+270_622+271delinsCT
NM_001386005.1:c.646+270_646+271delinsCT	NP_001372934.1:n.646+270_646+271delinsCT
NM_001386006.1:c.625+270_625+271delinsCT	NP_001372935.1:n.625+270_625+271delinsCT
NM_004001.5:c.646+270_646+271delinsCT	NP_003992.3:n.646+270_646+271delinsCT
NR_169827.1:n.875+270_875+271delinsCT
NM_001394477.1:c.646+270_646+271delinsCT MANE Select	NP_001381406.1:n.646+270_646+271delinsCT