Canonical Allele Identifier: CA10989170

Gene: FCGR2A

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161514774T>A , CM000663.2:g.161514774T>A	GRCh38
NC_000001.10:g.161484564T>A , CM000663.1:g.161484564T>A	GRCh37
NC_000001.9:g.159751188T>A	NCBI36
NG_012066.1:g.14360T>A
NG_012066.2:g.14360T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699277.1:c.657+842T>A	ENSP00000514258.1:n.657+842T>A
ENST00000699278.1:c.522+842T>A	ENSP00000514259.1:n.522+842T>A
ENST00000699279.1:c.363+842T>A	ENSP00000514260.1:n.363+842T>A
ENST00000271450.12:c.780+842T>A MANE Select	ENSP00000271450.6:n.780+842T>A
ENST00000271450.10:c.780+842T>A	ENSP00000271450.6:n.780+842T>A
ENST00000367972.8:c.777+842T>A	ENSP00000356949.4:n.777+842T>A
ENST00000459885.1:c.35+842T>A
ENST00000461298.1:n.189+842T>A
ENST00000467525.5:c.631-3201T>A	ENSP00000476495.1:n.631-3201T>A
ENST00000471026.5:n.350+842T>A
ENST00000483665.6:c.*482+842T>A	ENSP00000440148.1:n.*482+842T>A
ENST00000486608.1:n.155T>A
NM_001136219.1:c.780+842T>A	NP_001129691.1:n.780+842T>A
NM_021642.3:c.777+842T>A	NP_067674.2:n.777+842T>A
XM_011509287.1:c.780+842T>A	XP_011507589.1:n.780+842T>A
XM_011509288.1:c.777+842T>A	XP_011507590.1:n.777+842T>A
XM_011509289.1:c.657+842T>A	XP_011507591.1:n.657+842T>A
XM_011509290.1:c.780+842T>A	XP_011507592.1:n.780+842T>A
XM_011509291.1:c.743-3201T>A	XP_011507593.1:n.743-3201T>A
XM_011509287.2:c.780+842T>A	XP_011507589.1:n.780+842T>A
XM_011509290.2:c.780+842T>A	XP_011507592.1:n.780+842T>A
XM_017000663.2:c.777+842T>A	XP_016856152.1:n.777+842T>A
XM_017000664.1:c.780+842T>A	XP_016856153.1:n.780+842T>A
XM_017000665.1:c.780+842T>A	XP_016856154.1:n.780+842T>A
XM_017000666.1:c.657+842T>A	XP_016856155.1:n.657+842T>A
XM_017000667.1:c.657+842T>A	XP_016856156.1:n.657+842T>A
XM_017000668.2:c.654+842T>A	XP_016856157.1:n.654+842T>A
XM_024454040.1:c.363+842T>A	XP_024309808.1:n.363+842T>A
XM_024454041.1:c.363+842T>A	XP_024309809.1:n.363+842T>A
XR_001737042.1:n.818+842T>A
NM_001136219.3:c.780+842T>A MANE Select	NP_001129691.1:n.780+842T>A
NM_001375296.1:c.657+842T>A	NP_001362225.1:n.657+842T>A
NM_001375297.1:c.654+842T>A	NP_001362226.1:n.654+842T>A
NM_021642.5:c.777+842T>A	NP_067674.2:n.777+842T>A