Canonical Allele Identifier: CA1212509

Gene: FCGR3B

Linked Data

• dbSNP Id: rs200688856
• ExAC: 1:161599779 G / A
• gnomAD v2: 1-161599779-G-A
• gnomAD v3: 1-161629989-G-A
• gnomAD v4: 1-161629989-G-A
• MyVariant Identifiers: chr1:g.161599779G>A (hg19) ; chr1:g.161629989G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161629989G>A , CM000663.2:g.161629989G>A	GRCh38
NC_000001.10:g.161599779G>A , CM000663.1:g.161599779G>A	GRCh37
NC_000001.9:g.159866403G>A	NCBI36
NG_032926.1:g.6975C>T
NG_032926.2:g.6975C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000421702.4:c.105C>T	ENSP00000394204.3:p.Ser35=
ENST00000533780.2:n.484C>T
ENST00000699402.1:c.40+1066C>T	ENSP00000514363.1:n.40+1066C>T
ENST00000699403.1:c.61+379C>T	ENSP00000514364.1:n.61+379C>T
ENST00000699523.1:n.128-103C>T
ENST00000421702.3:c.105C>T	ENSP00000394204.3:p.Ser35=
ENST00000650385.1:c.108C>T MANE Select	ENSP00000497461.1:p.Ser36=
ENST00000294800.7:c.108C>T	ENSP00000294800.3:p.Ser36=
ENST00000367964.6:c.108C>T	ENSP00000356941.2:p.Ser36=
ENST00000421702.2:c.169C>T
ENST00000531221.5:c.216C>T	ENSP00000433642.1:p.Ser72=
ENST00000533780.1:n.262C>T
ENST00000534489.1:n.472C>T
ENST00000534776.1:c.57C>T	ENSP00000437084.1:p.Ser19=
ENST00000613418.4:c.57C>T	ENSP00000482838.1:p.Ser19=
ENST00000614870.4:c.57C>T	ENSP00000478466.1:p.Ser19=
NM_000570.4:c.108C>T	NP_000561.3:p.Ser36=
NM_001244753.1:c.216C>T	NP_001231682.1:p.Ser72=
NM_001271035.1:c.213C>T	NP_001257964.1:p.Ser71=
NM_001271036.1:c.57C>T	NP_001257965.1:p.Ser19=
NM_001271037.1:c.57C>T	NP_001257966.1:p.Ser19=
NM_001244753.2:c.108C>T MANE Select	NP_001231682.2:p.Ser36=
NM_001271035.2:c.105C>T	NP_001257964.2:p.Ser35=
NM_000570.5:c.108C>T	NP_000561.3:p.Ser36=
NM_001271036.2:c.57C>T	NP_001257965.1:p.Ser19=
NM_001271037.2:c.57C>T	NP_001257966.1:p.Ser19=