Canonical Allele Identifier: CA343347222

Gene: FCGR2A

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699277.1:c.500A>T	ENSP00000514258.1:p.His167Leu
ENST00000699278.1:c.242A>T	ENSP00000514259.1:p.His81Leu
ENST00000699279.1:c.83A>T	ENSP00000514260.1:p.His28Leu
ENST00000271450.12:c.500A>T MANE Select	ENSP00000271450.6:p.His167Leu
ENST00000271450.10:c.500A>T	ENSP00000271450.6:p.His167Leu
ENST00000367972.8:c.497A>T	ENSP00000356949.4:p.His166Leu
ENST00000467525.5:c.395A>T	ENSP00000476495.1:p.His132Leu
ENST00000467654.1:n.519A>T
ENST00000471026.5:n.193A>T
ENST00000483665.6:c.*202A>T	ENSP00000440148.1:n.*202A>T
NM_001136219.1:c.500A>T	NP_001129691.1:p.His167Leu
NM_021642.3:c.497A>T	NP_067674.2:p.His166Leu
XM_011509287.1:c.500A>T	XP_011507589.1:p.His167Leu
XM_011509288.1:c.497A>T	XP_011507590.1:p.His166Leu
XM_011509289.1:c.500A>T	XP_011507591.1:p.His167Leu
XM_011509290.1:c.500A>T	XP_011507592.1:p.His167Leu
XM_011509291.1:c.500A>T	XP_011507593.1:p.His167Leu
XM_011509287.2:c.500A>T	XP_011507589.1:p.His167Leu
XM_011509290.2:c.500A>T	XP_011507592.1:p.His167Leu
XM_017000663.2:c.497A>T	XP_016856152.1:p.His166Leu
XM_017000664.1:c.500A>T	XP_016856153.1:p.His167Leu
XM_017000665.1:c.500A>T	XP_016856154.1:p.His167Leu
XM_017000666.1:c.500A>T	XP_016856155.1:p.His167Leu
XM_017000667.1:c.500A>T	XP_016856156.1:p.His167Leu
XM_017000668.2:c.497A>T	XP_016856157.1:p.His166Leu
XM_024454040.1:c.83A>T	XP_024309808.1:p.His28Leu
XM_024454041.1:c.83A>T	XP_024309809.1:p.His28Leu
XR_001737042.1:n.538A>T
NM_001136219.3:c.500A>T MANE Select	NP_001129691.1:p.His167Leu
NM_001375296.1:c.500A>T	NP_001362225.1:p.His167Leu
NM_001375297.1:c.497A>T	NP_001362226.1:p.His166Leu
NM_021642.5:c.497A>T	NP_067674.2:p.His166Leu