Canonical Allele Identifier: CA421420710

Gene: FCGR2B

Linked Data

• gnomAD v4: 1-161674057-G-A
• MyVariant Identifiers: chr1:g.161643847G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161674057G>A , CM000663.2:g.161674057G>A	GRCh38
NC_000001.10:g.161643847G>A , CM000663.1:g.161643847G>A	GRCh37
NC_000001.9:g.159910471G>A	NCBI36
NG_023318.1:g.15943G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.744G>A MANE Select	ENSP00000351497.5:p.Arg248=
ENST00000236937.13:c.744G>A	ENSP00000236937.9:p.Arg248=
ENST00000358671.9:c.744G>A	ENSP00000351497.5:p.Arg248=
ENST00000367961.8:c.723G>A	ENSP00000356938.4:p.Arg241=
ENST00000428605.3:c.744G>A	ENSP00000404329.3:p.Arg248=
ENST00000480308.5:n.794G>A
ENST00000485778.1:n.2112G>A
NM_001002273.2:c.741G>A	NP_001002273.1:p.Arg247=
NM_001002274.2:c.744G>A	NP_001002274.1:p.Arg248=
NM_001002275.2:c.741G>A	NP_001002275.1:p.Arg247=
NM_001190828.1:c.723G>A	NP_001177757.1:p.Arg241=
NM_004001.4:c.744G>A	NP_003992.3:p.Arg248=
XM_017000670.2:c.741G>A	XP_016856159.1:p.Arg247=
XM_024454043.1:c.744G>A	XP_024309811.1:p.Arg248=
XM_024454044.1:c.741G>A	XP_024309812.1:p.Arg247=
XM_024454045.1:c.741G>A	XP_024309813.1:p.Arg247=
NM_001002273.3:c.741G>A	NP_001002273.1:p.Arg247=
NM_001002274.3:c.744G>A	NP_001002274.1:p.Arg248=
NM_001002275.3:c.741G>A	NP_001002275.1:p.Arg247=
NM_001190828.2:c.723G>A	NP_001177757.1:p.Arg241=
NM_001386000.1:c.720G>A	NP_001372929.1:p.Arg240=
NM_001386001.1:c.723G>A	NP_001372930.1:p.Arg241=
NM_001386002.1:c.720G>A	NP_001372931.1:p.Arg240=
NM_001386003.1:c.744G>A	NP_001372932.1:p.Arg248=
NM_001386004.1:c.720G>A	NP_001372933.1:p.Arg240=
NM_001386005.1:c.744G>A	NP_001372934.1:p.Arg248=
NM_001386006.1:c.723G>A	NP_001372935.1:p.Arg241=
NM_004001.5:c.744G>A	NP_003992.3:p.Arg248=
NR_169827.1:n.973G>A
NM_001394477.1:c.744G>A MANE Select	NP_001381406.1:p.Arg248=