Canonical Allele Identifier: CA1202839550

Gene: FCGR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161673535_161673536delinsTC , CM000663.2:g.161673535_161673536delinsTC	GRCh38
NC_000001.10:g.161643325_161643326delinsTC , CM000663.1:g.161643325_161643326delinsTC	GRCh37
NC_000001.9:g.159909949_159909950delinsTC	NCBI36
NG_023318.1:g.15421_15422delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.646+306_646+307delinsTC MANE Select	ENSP00000351497.5:n.646+306_646+307delinsTC
ENST00000236937.13:c.646+306_646+307delinsTC	ENSP00000236937.9:n.646+306_646+307delinsTC
ENST00000358671.9:c.646+306_646+307delinsTC	ENSP00000351497.5:n.646+306_646+307delinsTC
ENST00000367961.8:c.625+306_625+307delinsTC	ENSP00000356938.4:n.625+306_625+307delinsTC
ENST00000428605.3:c.646+306_646+307delinsTC	ENSP00000404329.3:n.646+306_646+307delinsTC
ENST00000480308.5:n.696+306_696+307delinsTC
ENST00000485778.1:n.2014+306_2014+307delinsTC
NM_001002273.2:c.643+306_643+307delinsTC	NP_001002273.1:n.643+306_643+307delinsTC
NM_001002274.2:c.646+306_646+307delinsTC	NP_001002274.1:n.646+306_646+307delinsTC
NM_001002275.2:c.643+306_643+307delinsTC	NP_001002275.1:n.643+306_643+307delinsTC
NM_001190828.1:c.625+306_625+307delinsTC	NP_001177757.1:n.625+306_625+307delinsTC
NM_004001.4:c.646+306_646+307delinsTC	NP_003992.3:n.646+306_646+307delinsTC
XM_011509292.1:c.*13_*14delinsTC	XP_011507594.1:n.*13_*14delinsTC
XM_017000670.2:c.643+306_643+307delinsTC	XP_016856159.1:n.643+306_643+307delinsTC
XM_024454043.1:c.646+306_646+307delinsTC	XP_024309811.1:n.646+306_646+307delinsTC
XM_024454044.1:c.643+306_643+307delinsTC	XP_024309812.1:n.643+306_643+307delinsTC
XM_024454045.1:c.643+306_643+307delinsTC	XP_024309813.1:n.643+306_643+307delinsTC
XM_024454047.1:c.*13_*14delinsTC	XP_024309815.1:n.*13_*14delinsTC
NM_001002273.3:c.643+306_643+307delinsTC	NP_001002273.1:n.643+306_643+307delinsTC
NM_001002274.3:c.646+306_646+307delinsTC	NP_001002274.1:n.646+306_646+307delinsTC
NM_001002275.3:c.643+306_643+307delinsTC	NP_001002275.1:n.643+306_643+307delinsTC
NM_001190828.2:c.625+306_625+307delinsTC	NP_001177757.1:n.625+306_625+307delinsTC
NM_001386000.1:c.622+306_622+307delinsTC	NP_001372929.1:n.622+306_622+307delinsTC
NM_001386001.1:c.625+306_625+307delinsTC	NP_001372930.1:n.625+306_625+307delinsTC
NM_001386002.1:c.622+306_622+307delinsTC	NP_001372931.1:n.622+306_622+307delinsTC
NM_001386003.1:c.646+306_646+307delinsTC	NP_001372932.1:n.646+306_646+307delinsTC
NM_001386004.1:c.622+306_622+307delinsTC	NP_001372933.1:n.622+306_622+307delinsTC
NM_001386005.1:c.646+306_646+307delinsTC	NP_001372934.1:n.646+306_646+307delinsTC
NM_001386006.1:c.625+306_625+307delinsTC	NP_001372935.1:n.625+306_625+307delinsTC
NM_004001.5:c.646+306_646+307delinsTC	NP_003992.3:n.646+306_646+307delinsTC
NR_169827.1:n.875+306_875+307delinsTC
NM_001394477.1:c.646+306_646+307delinsTC MANE Select	NP_001381406.1:n.646+306_646+307delinsTC