Canonical Allele Identifier: CA1139989882

Gene: FCGR2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161662856G= , CM000663.2:g.161662856G=	GRCh38
NC_000001.10:g.161632646G= , CM000663.1:g.161632646G=	GRCh37
NC_000001.9:g.159899270G=	NCBI36
NG_023318.1:g.4742G=

Transcript Alleles

HGVS	Amino-acid Change
XM_017000670.2:c.-72-314G=	XP_016856159.1:n.-72-314G=
XM_024454044.1:c.-72-314G=	XP_024309812.1:n.-72-314G=
XM_024454045.1:c.-72-314G=	XP_024309813.1:n.-72-314G=
XR_002959731.1:n.20-314G=
NM_001002273.3:c.-72-314G=	NP_001002273.1:n.-72-314G=
NM_001002274.3:c.-72-314G=	NP_001002274.1:n.-72-314G=
NM_001002275.3:c.-72-314G=	NP_001002275.1:n.-72-314G=
NM_001190828.2:c.-72-314G=	NP_001177757.1:n.-72-314G=
NM_001386000.1:c.-72-314G=	NP_001372929.1:n.-72-314G=
NM_001386001.1:c.-72-314G=	NP_001372930.1:n.-72-314G=
NM_001386002.1:c.-72-314G=	NP_001372931.1:n.-72-314G=
NM_001386003.1:c.-72-314G=	NP_001372932.1:n.-72-314G=
NM_001386004.1:c.-72-314G=	NP_001372933.1:n.-72-314G=
NM_001386005.1:c.-72-314G=	NP_001372934.1:n.-72-314G=
NM_001386006.1:c.-72-314G=	NP_001372935.1:n.-72-314G=
NM_004001.5:c.-72-314G=	NP_003992.3:n.-72-314G=
NR_169827.1:n.20-314G=