Canonical Allele Identifier: CA2648801980

Gene: FCGR2B

Linked Data

• gnomAD v4: 1-161674118-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161674121del , CM000663.2:g.161674121del	GRCh38
NC_000001.10:g.161643911del , CM000663.1:g.161643911del	GRCh37
NC_000001.9:g.159910535del	NCBI36
NG_023318.1:g.16007del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.760+48del MANE Select	ENSP00000351497.5:n.760+48del
ENST00000236937.13:c.760+48del	ENSP00000236937.9:n.760+48del
ENST00000358671.9:c.760+48del	ENSP00000351497.5:n.760+48del
ENST00000367961.8:c.739+48del	ENSP00000356938.4:n.739+48del
ENST00000428605.3:c.760+48del	ENSP00000404329.3:n.760+48del
ENST00000480308.5:n.858del
NM_001002273.2:c.757+48del	NP_001002273.1:n.757+48del
NM_001002274.2:c.760+48del	NP_001002274.1:n.760+48del
NM_001002275.2:c.757+48del	NP_001002275.1:n.757+48del
NM_001190828.1:c.739+48del	NP_001177757.1:n.739+48del
NM_004001.4:c.760+48del	NP_003992.3:n.760+48del
XM_017000670.2:c.757+48del	XP_016856159.1:n.757+48del
XM_024454043.1:c.760+48del	XP_024309811.1:n.760+48del
XM_024454044.1:c.757+48del	XP_024309812.1:n.757+48del
XM_024454045.1:c.757+48del	XP_024309813.1:n.757+48del
NM_001002273.3:c.757+48del	NP_001002273.1:n.757+48del
NM_001002274.3:c.760+48del	NP_001002274.1:n.760+48del
NM_001002275.3:c.757+48del	NP_001002275.1:n.757+48del
NM_001190828.2:c.739+48del	NP_001177757.1:n.739+48del
NM_001386000.1:c.736+48del	NP_001372929.1:n.736+48del
NM_001386001.1:c.739+48del	NP_001372930.1:n.739+48del
NM_001386002.1:c.736+48del	NP_001372931.1:n.736+48del
NM_001386003.1:c.760+48del	NP_001372932.1:n.760+48del
NM_001386004.1:c.736+48del	NP_001372933.1:n.736+48del
NM_001386005.1:c.760+48del	NP_001372934.1:n.760+48del
NM_001386006.1:c.739+48del	NP_001372935.1:n.739+48del
NM_004001.5:c.760+48del	NP_003992.3:n.760+48del
NR_169827.1:n.989+48del
NM_001394477.1:c.760+48del MANE Select	NP_001381406.1:n.760+48del