Canonical Allele Identifier: CA343367715
Gene: FCGR2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161674010G>A , CM000663.2:g.161674010G>A GRCh38
NC_000001.10:g.161643800G>A , CM000663.1:g.161643800G>A GRCh37
NC_000001.9:g.159910424G>A NCBI36
NG_023318.1:g.15896G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358671.10:c.697G>A MANE Select ENSP00000351497.5:p.Ala233Thr
ENST00000236937.13:c.697G>A ENSP00000236937.9:p.Ala233Thr
ENST00000358671.9:c.697G>A ENSP00000351497.5:p.Ala233Thr
ENST00000367961.8:c.676G>A ENSP00000356938.4:p.Ala226Thr
ENST00000428605.3:c.697G>A ENSP00000404329.3:p.Ala233Thr
ENST00000480308.5:n.747G>A
ENST00000485778.1:n.2065G>A
NM_001002273.2:c.694G>A NP_001002273.1:p.Ala232Thr
NM_001002274.2:c.697G>A NP_001002274.1:p.Ala233Thr
NM_001002275.2:c.694G>A NP_001002275.1:p.Ala232Thr
NM_001190828.1:c.676G>A NP_001177757.1:p.Ala226Thr
NM_004001.4:c.697G>A NP_003992.3:p.Ala233Thr
XM_017000670.2:c.694G>A XP_016856159.1:p.Ala232Thr
XM_024454043.1:c.697G>A XP_024309811.1:p.Ala233Thr
XM_024454044.1:c.694G>A XP_024309812.1:p.Ala232Thr
XM_024454045.1:c.694G>A XP_024309813.1:p.Ala232Thr
NM_001002273.3:c.694G>A NP_001002273.1:p.Ala232Thr
NM_001002274.3:c.697G>A NP_001002274.1:p.Ala233Thr
NM_001002275.3:c.694G>A NP_001002275.1:p.Ala232Thr
NM_001190828.2:c.676G>A NP_001177757.1:p.Ala226Thr
NM_001386000.1:c.673G>A NP_001372929.1:p.Ala225Thr
NM_001386001.1:c.676G>A NP_001372930.1:p.Ala226Thr
NM_001386002.1:c.673G>A NP_001372931.1:p.Ala225Thr
NM_001386003.1:c.697G>A NP_001372932.1:p.Ala233Thr
NM_001386004.1:c.673G>A NP_001372933.1:p.Ala225Thr
NM_001386005.1:c.697G>A NP_001372934.1:p.Ala233Thr
NM_001386006.1:c.676G>A NP_001372935.1:p.Ala226Thr
NM_004001.5:c.697G>A NP_003992.3:p.Ala233Thr
NR_169827.1:n.926G>A
NM_001394477.1:c.697G>A MANE Select NP_001381406.1:p.Ala233Thr