Canonical Allele Identifier: CA2648801447

Gene: FCGR2B

Linked Data

• gnomAD v4: 1-161673496-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161673496T>C , CM000663.2:g.161673496T>C	GRCh38
NC_000001.10:g.161643286T>C , CM000663.1:g.161643286T>C	GRCh37
NC_000001.9:g.159909910T>C	NCBI36
NG_023318.1:g.15382T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.646+267T>C MANE Select	ENSP00000351497.5:n.646+267T>C
ENST00000236937.13:c.646+267T>C	ENSP00000236937.9:n.646+267T>C
ENST00000358671.9:c.646+267T>C	ENSP00000351497.5:n.646+267T>C
ENST00000367961.8:c.625+267T>C	ENSP00000356938.4:n.625+267T>C
ENST00000428605.3:c.646+267T>C	ENSP00000404329.3:n.646+267T>C
ENST00000480308.5:n.696+267T>C
ENST00000485778.1:n.2014+267T>C
NM_001002273.2:c.643+267T>C	NP_001002273.1:n.643+267T>C
NM_001002274.2:c.646+267T>C	NP_001002274.1:n.646+267T>C
NM_001002275.2:c.643+267T>C	NP_001002275.1:n.643+267T>C
NM_001190828.1:c.625+267T>C	NP_001177757.1:n.625+267T>C
NM_004001.4:c.646+267T>C	NP_003992.3:n.646+267T>C
XM_011509292.1:c.679T>C	XP_011507594.1:p.Ser227Pro
XM_017000670.2:c.643+267T>C	XP_016856159.1:n.643+267T>C
XM_024454043.1:c.646+267T>C	XP_024309811.1:n.646+267T>C
XM_024454044.1:c.643+267T>C	XP_024309812.1:n.643+267T>C
XM_024454045.1:c.643+267T>C	XP_024309813.1:n.643+267T>C
XM_024454047.1:c.679T>C	XP_024309815.1:p.Ser227Pro
NM_001002273.3:c.643+267T>C	NP_001002273.1:n.643+267T>C
NM_001002274.3:c.646+267T>C	NP_001002274.1:n.646+267T>C
NM_001002275.3:c.643+267T>C	NP_001002275.1:n.643+267T>C
NM_001190828.2:c.625+267T>C	NP_001177757.1:n.625+267T>C
NM_001386000.1:c.622+267T>C	NP_001372929.1:n.622+267T>C
NM_001386001.1:c.625+267T>C	NP_001372930.1:n.625+267T>C
NM_001386002.1:c.622+267T>C	NP_001372931.1:n.622+267T>C
NM_001386003.1:c.646+267T>C	NP_001372932.1:n.646+267T>C
NM_001386004.1:c.622+267T>C	NP_001372933.1:n.622+267T>C
NM_001386005.1:c.646+267T>C	NP_001372934.1:n.646+267T>C
NM_001386006.1:c.625+267T>C	NP_001372935.1:n.625+267T>C
NM_004001.5:c.646+267T>C	NP_003992.3:n.646+267T>C
NR_169827.1:n.875+267T>C
NM_001394477.1:c.646+267T>C MANE Select	NP_001381406.1:n.646+267T>C