Canonical Allele Identifier: CA343368190

Gene: FCGR2B

Linked Data

• MyVariant Identifiers: chr1:g.161643858T>C (hg19) ; chr1:g.161674068T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161674068T>C , CM000663.2:g.161674068T>C	GRCh38
NC_000001.10:g.161643858T>C , CM000663.1:g.161643858T>C	GRCh37
NC_000001.9:g.159910482T>C	NCBI36
NG_023318.1:g.15954T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.755T>C MANE Select	ENSP00000351497.5:p.Ile252Thr
ENST00000236937.13:c.755T>C	ENSP00000236937.9:p.Ile252Thr
ENST00000358671.9:c.755T>C	ENSP00000351497.5:p.Ile252Thr
ENST00000367961.8:c.734T>C	ENSP00000356938.4:p.Ile245Thr
ENST00000428605.3:c.755T>C	ENSP00000404329.3:p.Ile252Thr
ENST00000480308.5:n.805T>C
ENST00000485778.1:n.2123T>C
NM_001002273.2:c.752T>C	NP_001002273.1:p.Ile251Thr
NM_001002274.2:c.755T>C	NP_001002274.1:p.Ile252Thr
NM_001002275.2:c.752T>C	NP_001002275.1:p.Ile251Thr
NM_001190828.1:c.734T>C	NP_001177757.1:p.Ile245Thr
NM_004001.4:c.755T>C	NP_003992.3:p.Ile252Thr
XM_017000670.2:c.752T>C	XP_016856159.1:p.Ile251Thr
XM_024454043.1:c.755T>C	XP_024309811.1:p.Ile252Thr
XM_024454044.1:c.752T>C	XP_024309812.1:p.Ile251Thr
XM_024454045.1:c.752T>C	XP_024309813.1:p.Ile251Thr
NM_001002273.3:c.752T>C	NP_001002273.1:p.Ile251Thr
NM_001002274.3:c.755T>C	NP_001002274.1:p.Ile252Thr
NM_001002275.3:c.752T>C	NP_001002275.1:p.Ile251Thr
NM_001190828.2:c.734T>C	NP_001177757.1:p.Ile245Thr
NM_001386000.1:c.731T>C	NP_001372929.1:p.Ile244Thr
NM_001386001.1:c.734T>C	NP_001372930.1:p.Ile245Thr
NM_001386002.1:c.731T>C	NP_001372931.1:p.Ile244Thr
NM_001386003.1:c.755T>C	NP_001372932.1:p.Ile252Thr
NM_001386004.1:c.731T>C	NP_001372933.1:p.Ile244Thr
NM_001386005.1:c.755T>C	NP_001372934.1:p.Ile252Thr
NM_001386006.1:c.734T>C	NP_001372935.1:p.Ile245Thr
NM_004001.5:c.755T>C	NP_003992.3:p.Ile252Thr
NR_169827.1:n.984T>C
NM_001394477.1:c.755T>C MANE Select	NP_001381406.1:p.Ile252Thr