Canonical Allele Identifier: CA343367751
Gene: FCGR2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161674014T>C , CM000663.2:g.161674014T>C GRCh38
NC_000001.10:g.161643804T>C , CM000663.1:g.161643804T>C GRCh37
NC_000001.9:g.159910428T>C NCBI36
NG_023318.1:g.15900T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000358671.10:c.701T>C MANE Select ENSP00000351497.5:p.Val234Ala
ENST00000236937.13:c.701T>C ENSP00000236937.9:p.Val234Ala
ENST00000358671.9:c.701T>C ENSP00000351497.5:p.Val234Ala
ENST00000367961.8:c.680T>C ENSP00000356938.4:p.Val227Ala
ENST00000428605.3:c.701T>C ENSP00000404329.3:p.Val234Ala
ENST00000480308.5:n.751T>C
ENST00000485778.1:n.2069T>C
NM_001002273.2:c.698T>C NP_001002273.1:p.Val233Ala
NM_001002274.2:c.701T>C NP_001002274.1:p.Val234Ala
NM_001002275.2:c.698T>C NP_001002275.1:p.Val233Ala
NM_001190828.1:c.680T>C NP_001177757.1:p.Val227Ala
NM_004001.4:c.701T>C NP_003992.3:p.Val234Ala
XM_017000670.2:c.698T>C XP_016856159.1:p.Val233Ala
XM_024454043.1:c.701T>C XP_024309811.1:p.Val234Ala
XM_024454044.1:c.698T>C XP_024309812.1:p.Val233Ala
XM_024454045.1:c.698T>C XP_024309813.1:p.Val233Ala
NM_001002273.3:c.698T>C NP_001002273.1:p.Val233Ala
NM_001002274.3:c.701T>C NP_001002274.1:p.Val234Ala
NM_001002275.3:c.698T>C NP_001002275.1:p.Val233Ala
NM_001190828.2:c.680T>C NP_001177757.1:p.Val227Ala
NM_001386000.1:c.677T>C NP_001372929.1:p.Val226Ala
NM_001386001.1:c.680T>C NP_001372930.1:p.Val227Ala
NM_001386002.1:c.677T>C NP_001372931.1:p.Val226Ala
NM_001386003.1:c.701T>C NP_001372932.1:p.Val234Ala
NM_001386004.1:c.677T>C NP_001372933.1:p.Val226Ala
NM_001386005.1:c.701T>C NP_001372934.1:p.Val234Ala
NM_001386006.1:c.680T>C NP_001372935.1:p.Val227Ala
NM_004001.5:c.701T>C NP_003992.3:p.Val234Ala
NR_169827.1:n.930T>C
NM_001394477.1:c.701T>C MANE Select NP_001381406.1:p.Val234Ala