Canonical Allele Identifier: CA343352323

Gene: FCGR3B

Linked Data

• dbSNP Id: rs448740
• gnomAD v3: 1-161629903-T-A
• gnomAD v4: 1-161629903-T-A
• MyVariant Identifiers: chr1:g.161599693T>A (hg19) ; chr1:g.161629903T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161629903T>A , CM000663.2:g.161629903T>A	GRCh38
NC_000001.10:g.161599693T>A , CM000663.1:g.161599693T>A	GRCh37
NC_000001.9:g.159866317T>A	NCBI36
NG_032926.1:g.7061A>T
NG_032926.2:g.7061A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421702.4:c.191A>T	ENSP00000394204.3:p.Asn64Ile
ENST00000533780.2:n.570A>T
ENST00000699402.1:c.40+1152A>T	ENSP00000514363.1:n.40+1152A>T
ENST00000699403.1:c.61+465A>T	ENSP00000514364.1:n.61+465A>T
ENST00000699523.1:n.128-17A>T
ENST00000421702.3:c.191A>T	ENSP00000394204.3:p.Asn64Ile
ENST00000650385.1:c.194A>T MANE Select	ENSP00000497461.1:p.Asn65Ile
ENST00000294800.7:c.194A>T	ENSP00000294800.3:p.Asn65Ile
ENST00000367964.6:c.194A>T	ENSP00000356941.2:p.Asn65Ile
ENST00000421702.2:c.255A>T
ENST00000531221.5:c.302A>T	ENSP00000433642.1:p.Asn101Ile
ENST00000533780.1:n.348A>T
ENST00000534489.1:n.558A>T
ENST00000534776.1:c.143A>T	ENSP00000437084.1:p.Asn48Ile
ENST00000613418.4:c.143A>T	ENSP00000482838.1:p.Asn48Ile
ENST00000614870.4:c.143A>T	ENSP00000478466.1:p.Asn48Ile
NM_000570.4:c.194A>T	NP_000561.3:p.Asn65Ile
NM_001244753.1:c.302A>T	NP_001231682.1:p.Asn101Ile
NM_001271035.1:c.299A>T	NP_001257964.1:p.Asn100Ile
NM_001271036.1:c.143A>T	NP_001257965.1:p.Asn48Ile
NM_001271037.1:c.143A>T	NP_001257966.1:p.Asn48Ile
NM_001244753.2:c.194A>T MANE Select	NP_001231682.2:p.Asn65Ile
NM_001271035.2:c.191A>T	NP_001257964.2:p.Asn64Ile
NM_000570.5:c.194A>T	NP_000561.3:p.Asn65Ile
NM_001271036.2:c.143A>T	NP_001257965.1:p.Asn48Ile
NM_001271037.2:c.143A>T	NP_001257966.1:p.Asn48Ile