Canonical Allele Identifier: CA343367623

Gene: FCGR2B

Linked Data

• dbSNP Id: rs1294388116
• gnomAD v2: 1-161643783-C-T
• gnomAD v4: 1-161673993-C-T
• MyVariant Identifiers: chr1:g.161643783C>T (hg19) ; chr1:g.161673993C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161673993C>T , CM000663.2:g.161673993C>T	GRCh38
NC_000001.10:g.161643783C>T , CM000663.1:g.161643783C>T	GRCh37
NC_000001.9:g.159910407C>T	NCBI36
NG_023318.1:g.15879C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.680C>T MANE Select	ENSP00000351497.5:p.Ala227Val
ENST00000236937.13:c.680C>T	ENSP00000236937.9:p.Ala227Val
ENST00000358671.9:c.680C>T	ENSP00000351497.5:p.Ala227Val
ENST00000367961.8:c.659C>T	ENSP00000356938.4:p.Ala220Val
ENST00000428605.3:c.680C>T	ENSP00000404329.3:p.Ala227Val
ENST00000480308.5:n.730C>T
ENST00000485778.1:n.2048C>T
NM_001002273.2:c.677C>T	NP_001002273.1:p.Ala226Val
NM_001002274.2:c.680C>T	NP_001002274.1:p.Ala227Val
NM_001002275.2:c.677C>T	NP_001002275.1:p.Ala226Val
NM_001190828.1:c.659C>T	NP_001177757.1:p.Ala220Val
NM_004001.4:c.680C>T	NP_003992.3:p.Ala227Val
XM_017000670.2:c.677C>T	XP_016856159.1:p.Ala226Val
XM_024454043.1:c.680C>T	XP_024309811.1:p.Ala227Val
XM_024454044.1:c.677C>T	XP_024309812.1:p.Ala226Val
XM_024454045.1:c.677C>T	XP_024309813.1:p.Ala226Val
NM_001002273.3:c.677C>T	NP_001002273.1:p.Ala226Val
NM_001002274.3:c.680C>T	NP_001002274.1:p.Ala227Val
NM_001002275.3:c.677C>T	NP_001002275.1:p.Ala226Val
NM_001190828.2:c.659C>T	NP_001177757.1:p.Ala220Val
NM_001386000.1:c.656C>T	NP_001372929.1:p.Ala219Val
NM_001386001.1:c.659C>T	NP_001372930.1:p.Ala220Val
NM_001386002.1:c.656C>T	NP_001372931.1:p.Ala219Val
NM_001386003.1:c.680C>T	NP_001372932.1:p.Ala227Val
NM_001386004.1:c.656C>T	NP_001372933.1:p.Ala219Val
NM_001386005.1:c.680C>T	NP_001372934.1:p.Ala227Val
NM_001386006.1:c.659C>T	NP_001372935.1:p.Ala220Val
NM_004001.5:c.680C>T	NP_003992.3:p.Ala227Val
NR_169827.1:n.909C>T
NM_001394477.1:c.680C>T MANE Select	NP_001381406.1:p.Ala227Val