Canonical Allele Identifier: CA421420308
Gene: FCGR2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.161643751T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161673961T>A , CM000663.2:g.161673961T>A GRCh38
NC_000001.10:g.161643751T>A , CM000663.1:g.161643751T>A GRCh37
NC_000001.9:g.159910375T>A NCBI36
NG_023318.1:g.15847T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358671.10:c.648T>A MANE Select ENSP00000351497.5:p.Ala216=
ENST00000236937.13:c.648T>A ENSP00000236937.9:p.Ala216=
ENST00000358671.9:c.648T>A ENSP00000351497.5:p.Ala216=
ENST00000367961.8:c.627T>A ENSP00000356938.4:p.Ala209=
ENST00000428605.3:c.648T>A ENSP00000404329.3:p.Ala216=
ENST00000480308.5:n.698T>A
ENST00000485778.1:n.2016T>A
NM_001002273.2:c.645T>A NP_001002273.1:p.Ala215=
NM_001002274.2:c.648T>A NP_001002274.1:p.Ala216=
NM_001002275.2:c.645T>A NP_001002275.1:p.Ala215=
NM_001190828.1:c.627T>A NP_001177757.1:p.Ala209=
NM_004001.4:c.648T>A NP_003992.3:p.Ala216=
XM_017000670.2:c.645T>A XP_016856159.1:p.Ala215=
XM_024454043.1:c.648T>A XP_024309811.1:p.Ala216=
XM_024454044.1:c.645T>A XP_024309812.1:p.Ala215=
XM_024454045.1:c.645T>A XP_024309813.1:p.Ala215=
NM_001002273.3:c.645T>A NP_001002273.1:p.Ala215=
NM_001002274.3:c.648T>A NP_001002274.1:p.Ala216=
NM_001002275.3:c.645T>A NP_001002275.1:p.Ala215=
NM_001190828.2:c.627T>A NP_001177757.1:p.Ala209=
NM_001386000.1:c.624T>A NP_001372929.1:p.Ala208=
NM_001386001.1:c.627T>A NP_001372930.1:p.Ala209=
NM_001386002.1:c.624T>A NP_001372931.1:p.Ala208=
NM_001386003.1:c.648T>A NP_001372932.1:p.Ala216=
NM_001386004.1:c.624T>A NP_001372933.1:p.Ala208=
NM_001386005.1:c.648T>A NP_001372934.1:p.Ala216=
NM_001386006.1:c.627T>A NP_001372935.1:p.Ala209=
NM_004001.5:c.648T>A NP_003992.3:p.Ala216=
NR_169827.1:n.877T>A
NM_001394477.1:c.648T>A MANE Select NP_001381406.1:p.Ala216=