Canonical Allele Identifier: CA343367812

Gene: FCGR2B

Linked Data

• MyVariant Identifiers: chr1:g.161643813T>C (hg19) ; chr1:g.161674023T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161674023T>C , CM000663.2:g.161674023T>C	GRCh38
NC_000001.10:g.161643813T>C , CM000663.1:g.161643813T>C	GRCh37
NC_000001.9:g.159910437T>C	NCBI36
NG_023318.1:g.15909T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000358671.10:c.710T>C MANE Select	ENSP00000351497.5:p.Ile237Thr
ENST00000236937.13:c.710T>C	ENSP00000236937.9:p.Ile237Thr
ENST00000358671.9:c.710T>C	ENSP00000351497.5:p.Ile237Thr
ENST00000367961.8:c.689T>C	ENSP00000356938.4:p.Ile230Thr
ENST00000428605.3:c.710T>C	ENSP00000404329.3:p.Ile237Thr
ENST00000480308.5:n.760T>C
ENST00000485778.1:n.2078T>C
NM_001002273.2:c.707T>C	NP_001002273.1:p.Ile236Thr
NM_001002274.2:c.710T>C	NP_001002274.1:p.Ile237Thr
NM_001002275.2:c.707T>C	NP_001002275.1:p.Ile236Thr
NM_001190828.1:c.689T>C	NP_001177757.1:p.Ile230Thr
NM_004001.4:c.710T>C	NP_003992.3:p.Ile237Thr
XM_017000670.2:c.707T>C	XP_016856159.1:p.Ile236Thr
XM_024454043.1:c.710T>C	XP_024309811.1:p.Ile237Thr
XM_024454044.1:c.707T>C	XP_024309812.1:p.Ile236Thr
XM_024454045.1:c.707T>C	XP_024309813.1:p.Ile236Thr
NM_001002273.3:c.707T>C	NP_001002273.1:p.Ile236Thr
NM_001002274.3:c.710T>C	NP_001002274.1:p.Ile237Thr
NM_001002275.3:c.707T>C	NP_001002275.1:p.Ile236Thr
NM_001190828.2:c.689T>C	NP_001177757.1:p.Ile230Thr
NM_001386000.1:c.686T>C	NP_001372929.1:p.Ile229Thr
NM_001386001.1:c.689T>C	NP_001372930.1:p.Ile230Thr
NM_001386002.1:c.686T>C	NP_001372931.1:p.Ile229Thr
NM_001386003.1:c.710T>C	NP_001372932.1:p.Ile237Thr
NM_001386004.1:c.686T>C	NP_001372933.1:p.Ile229Thr
NM_001386005.1:c.710T>C	NP_001372934.1:p.Ile237Thr
NM_001386006.1:c.689T>C	NP_001372935.1:p.Ile230Thr
NM_004001.5:c.710T>C	NP_003992.3:p.Ile237Thr
NR_169827.1:n.939T>C
NM_001394477.1:c.710T>C MANE Select	NP_001381406.1:p.Ile237Thr