Canonical Allele Identifier: CA421420477

Gene: FCGR2B

Linked Data

• MyVariant Identifiers: chr1:g.161643790C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161674000C>G , CM000663.2:g.161674000C>G	GRCh38
NC_000001.10:g.161643790C>G , CM000663.1:g.161643790C>G	GRCh37
NC_000001.9:g.159910414C>G	NCBI36
NG_023318.1:g.15886C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358671.10:c.687C>G MANE Select	ENSP00000351497.5:p.Val229=
ENST00000236937.13:c.687C>G	ENSP00000236937.9:p.Val229=
ENST00000358671.9:c.687C>G	ENSP00000351497.5:p.Val229=
ENST00000367961.8:c.666C>G	ENSP00000356938.4:p.Val222=
ENST00000428605.3:c.687C>G	ENSP00000404329.3:p.Val229=
ENST00000480308.5:n.737C>G
ENST00000485778.1:n.2055C>G
NM_001002273.2:c.684C>G	NP_001002273.1:p.Val228=
NM_001002274.2:c.687C>G	NP_001002274.1:p.Val229=
NM_001002275.2:c.684C>G	NP_001002275.1:p.Val228=
NM_001190828.1:c.666C>G	NP_001177757.1:p.Val222=
NM_004001.4:c.687C>G	NP_003992.3:p.Val229=
XM_017000670.2:c.684C>G	XP_016856159.1:p.Val228=
XM_024454043.1:c.687C>G	XP_024309811.1:p.Val229=
XM_024454044.1:c.684C>G	XP_024309812.1:p.Val228=
XM_024454045.1:c.684C>G	XP_024309813.1:p.Val228=
NM_001002273.3:c.684C>G	NP_001002273.1:p.Val228=
NM_001002274.3:c.687C>G	NP_001002274.1:p.Val229=
NM_001002275.3:c.684C>G	NP_001002275.1:p.Val228=
NM_001190828.2:c.666C>G	NP_001177757.1:p.Val222=
NM_001386000.1:c.663C>G	NP_001372929.1:p.Val221=
NM_001386001.1:c.666C>G	NP_001372930.1:p.Val222=
NM_001386002.1:c.663C>G	NP_001372931.1:p.Val221=
NM_001386003.1:c.687C>G	NP_001372932.1:p.Val229=
NM_001386004.1:c.663C>G	NP_001372933.1:p.Val221=
NM_001386005.1:c.687C>G	NP_001372934.1:p.Val229=
NM_001386006.1:c.666C>G	NP_001372935.1:p.Val222=
NM_004001.5:c.687C>G	NP_003992.3:p.Val229=
NR_169827.1:n.916C>G
NM_001394477.1:c.687C>G MANE Select	NP_001381406.1:p.Val229=