Canonical Allele Identifier: CA343347216
Gene: FCGR2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161509955A>C , CM000663.2:g.161509955A>C GRCh38
NC_000001.10:g.161479745A>C , CM000663.1:g.161479745A>C GRCh37
NC_000001.9:g.159746369A>C NCBI36
NG_012066.1:g.9541A>C
NG_012066.2:g.9541A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699277.1:c.500A>C ENSP00000514258.1:p.His167Pro
ENST00000699278.1:c.242A>C ENSP00000514259.1:p.His81Pro
ENST00000699279.1:c.83A>C ENSP00000514260.1:p.His28Pro
ENST00000271450.12:c.500A>C MANE Select ENSP00000271450.6:p.His167Pro
ENST00000271450.10:c.500A>C ENSP00000271450.6:p.His167Pro
ENST00000367972.8:c.497A>C ENSP00000356949.4:p.His166Pro
ENST00000467525.5:c.395A>C ENSP00000476495.1:p.His132Pro
ENST00000467654.1:n.519A>C
ENST00000471026.5:n.193A>C
ENST00000483665.6:c.*202A>C ENSP00000440148.1:n.*202A>C
NM_001136219.1:c.500A>C NP_001129691.1:p.His167Pro
NM_021642.3:c.497A>C NP_067674.2:p.His166Pro
XM_011509287.1:c.500A>C XP_011507589.1:p.His167Pro
XM_011509288.1:c.497A>C XP_011507590.1:p.His166Pro
XM_011509289.1:c.500A>C XP_011507591.1:p.His167Pro
XM_011509290.1:c.500A>C XP_011507592.1:p.His167Pro
XM_011509291.1:c.500A>C XP_011507593.1:p.His167Pro
XM_011509287.2:c.500A>C XP_011507589.1:p.His167Pro
XM_011509290.2:c.500A>C XP_011507592.1:p.His167Pro
XM_017000663.2:c.497A>C XP_016856152.1:p.His166Pro
XM_017000664.1:c.500A>C XP_016856153.1:p.His167Pro
XM_017000665.1:c.500A>C XP_016856154.1:p.His167Pro
XM_017000666.1:c.500A>C XP_016856155.1:p.His167Pro
XM_017000667.1:c.500A>C XP_016856156.1:p.His167Pro
XM_017000668.2:c.497A>C XP_016856157.1:p.His166Pro
XM_024454040.1:c.83A>C XP_024309808.1:p.His28Pro
XM_024454041.1:c.83A>C XP_024309809.1:p.His28Pro
XR_001737042.1:n.538A>C
NM_001136219.3:c.500A>C MANE Select NP_001129691.1:p.His167Pro
NM_001375296.1:c.500A>C NP_001362225.1:p.His167Pro
NM_001375297.1:c.497A>C NP_001362226.1:p.His166Pro
NM_021642.5:c.497A>C NP_067674.2:p.His166Pro
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