Canonical Allele Identifier: CA526888618
Gene: FCGR2B HGNC NCBI

Linked Data

dbSNP Id: rs1163841391

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161673937G>A , CM000663.2:g.161673937G>A GRCh38
NC_000001.10:g.161643727G>A , CM000663.1:g.161643727G>A GRCh37
NC_000001.9:g.159910351G>A NCBI36
NG_023318.1:g.15823G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358671.10:c.647-23G>A MANE Select ENSP00000351497.5:n.647-23G>A
ENST00000236937.13:c.647-23G>A ENSP00000236937.9:n.647-23G>A
ENST00000358671.9:c.647-23G>A ENSP00000351497.5:n.647-23G>A
ENST00000367961.8:c.626-23G>A ENSP00000356938.4:n.626-23G>A
ENST00000428605.3:c.647-23G>A ENSP00000404329.3:n.647-23G>A
ENST00000480308.5:n.697-23G>A
ENST00000485778.1:n.2015-23G>A
NM_001002273.2:c.644-23G>A NP_001002273.1:n.644-23G>A
NM_001002274.2:c.647-23G>A NP_001002274.1:n.647-23G>A
NM_001002275.2:c.644-23G>A NP_001002275.1:n.644-23G>A
NM_001190828.1:c.626-23G>A NP_001177757.1:n.626-23G>A
NM_004001.4:c.647-23G>A NP_003992.3:n.647-23G>A
XM_017000670.2:c.644-23G>A XP_016856159.1:n.644-23G>A
XM_024454043.1:c.647-23G>A XP_024309811.1:n.647-23G>A
XM_024454044.1:c.644-23G>A XP_024309812.1:n.644-23G>A
XM_024454045.1:c.644-23G>A XP_024309813.1:n.644-23G>A
NM_001002273.3:c.644-23G>A NP_001002273.1:n.644-23G>A
NM_001002274.3:c.647-23G>A NP_001002274.1:n.647-23G>A
NM_001002275.3:c.644-23G>A NP_001002275.1:n.644-23G>A
NM_001190828.2:c.626-23G>A NP_001177757.1:n.626-23G>A
NM_001386000.1:c.623-23G>A NP_001372929.1:n.623-23G>A
NM_001386001.1:c.626-23G>A NP_001372930.1:n.626-23G>A
NM_001386002.1:c.623-23G>A NP_001372931.1:n.623-23G>A
NM_001386003.1:c.647-23G>A NP_001372932.1:n.647-23G>A
NM_001386004.1:c.623-23G>A NP_001372933.1:n.623-23G>A
NM_001386005.1:c.647-23G>A NP_001372934.1:n.647-23G>A
NM_001386006.1:c.626-23G>A NP_001372935.1:n.626-23G>A
NM_004001.5:c.647-23G>A NP_003992.3:n.647-23G>A
NR_169827.1:n.876-23G>A
NM_001394477.1:c.647-23G>A MANE Select NP_001381406.1:n.647-23G>A