Canonical Allele Identifier: CA2746388943

Gene: FCGR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161673805_161673806insGGTTT , CM000663.2:g.161673805_161673806insGGTTT	GRCh38
NC_000001.10:g.161643595_161643596insGGTTT , CM000663.1:g.161643595_161643596insGGTTT	GRCh37
NC_000001.9:g.159910219_159910220insGGTTT	NCBI36
NG_023318.1:g.15691_15692insGGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.647-155_647-154insGGTTT MANE Select	ENSP00000351497.5:n.647-155_647-154insGGTTT
ENST00000236937.13:c.647-155_647-154insGGTTT	ENSP00000236937.9:n.647-155_647-154insGGTTT
ENST00000358671.9:c.647-155_647-154insGGTTT	ENSP00000351497.5:n.647-155_647-154insGGTTT
ENST00000367961.8:c.626-155_626-154insGGTTT	ENSP00000356938.4:n.626-155_626-154insGGTTT
ENST00000428605.3:c.647-155_647-154insGGTTT	ENSP00000404329.3:n.647-155_647-154insGGTTT
ENST00000480308.5:n.697-155_697-154insGGTTT
ENST00000485778.1:n.2015-155_2015-154insGGTTT
NM_001002273.2:c.644-155_644-154insGGTTT	NP_001002273.1:n.644-155_644-154insGGTTT
NM_001002274.2:c.647-155_647-154insGGTTT	NP_001002274.1:n.647-155_647-154insGGTTT
NM_001002275.2:c.644-155_644-154insGGTTT	NP_001002275.1:n.644-155_644-154insGGTTT
NM_001190828.1:c.626-155_626-154insGGTTT	NP_001177757.1:n.626-155_626-154insGGTTT
NM_004001.4:c.647-155_647-154insGGTTT	NP_003992.3:n.647-155_647-154insGGTTT
XM_017000670.2:c.644-155_644-154insGGTTT	XP_016856159.1:n.644-155_644-154insGGTTT
XM_024454043.1:c.647-155_647-154insGGTTT	XP_024309811.1:n.647-155_647-154insGGTTT
XM_024454044.1:c.644-155_644-154insGGTTT	XP_024309812.1:n.644-155_644-154insGGTTT
XM_024454045.1:c.644-155_644-154insGGTTT	XP_024309813.1:n.644-155_644-154insGGTTT
NM_001002273.3:c.644-155_644-154insGGTTT	NP_001002273.1:n.644-155_644-154insGGTTT
NM_001002274.3:c.647-155_647-154insGGTTT	NP_001002274.1:n.647-155_647-154insGGTTT
NM_001002275.3:c.644-155_644-154insGGTTT	NP_001002275.1:n.644-155_644-154insGGTTT
NM_001190828.2:c.626-155_626-154insGGTTT	NP_001177757.1:n.626-155_626-154insGGTTT
NM_001386000.1:c.623-155_623-154insGGTTT	NP_001372929.1:n.623-155_623-154insGGTTT
NM_001386001.1:c.626-155_626-154insGGTTT	NP_001372930.1:n.626-155_626-154insGGTTT
NM_001386002.1:c.623-155_623-154insGGTTT	NP_001372931.1:n.623-155_623-154insGGTTT
NM_001386003.1:c.647-155_647-154insGGTTT	NP_001372932.1:n.647-155_647-154insGGTTT
NM_001386004.1:c.623-155_623-154insGGTTT	NP_001372933.1:n.623-155_623-154insGGTTT
NM_001386005.1:c.647-155_647-154insGGTTT	NP_001372934.1:n.647-155_647-154insGGTTT
NM_001386006.1:c.626-155_626-154insGGTTT	NP_001372935.1:n.626-155_626-154insGGTTT
NM_004001.5:c.647-155_647-154insGGTTT	NP_003992.3:n.647-155_647-154insGGTTT
NR_169827.1:n.876-155_876-154insGGTTT
NM_001394477.1:c.647-155_647-154insGGTTT MANE Select	NP_001381406.1:n.647-155_647-154insGGTTT