Canonical Allele Identifier: CA526879467

Gene: FCGR2A

Linked Data

• dbSNP Id: rs1326987389
• gnomAD v2: 1-161490965-T-G
• gnomAD v3: 1-161521175-T-G
• gnomAD v4: 1-161521175-T-G
• MyVariant Identifiers: chr1:g.161490965T>G (hg19) ; chr1:g.161521175T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161521175T>G , CM000663.2:g.161521175T>G	GRCh38
NC_000001.10:g.161490965T>G , CM000663.1:g.161490965T>G	GRCh37
NC_000001.9:g.159757589T>G	NCBI36
NG_012066.1:g.20761T>G
NG_012066.2:g.20761T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467525.5:c.918+1462T>G	ENSP00000476495.1:n.918+1462T>G
ENST00000491841.1:n.425+1184T>G
XM_011509287.1:c.*23+1184T>G	XP_011507589.1:n.*23+1184T>G
XM_011509288.1:c.*23+1184T>G	XP_011507590.1:n.*23+1184T>G
XM_011509289.1:c.*23+1184T>G	XP_011507591.1:n.*23+1184T>G
XM_011509287.2:c.*23+1184T>G	XP_011507589.1:n.*23+1184T>G
XM_017000664.1:c.944-2115T>G	XP_016856153.1:n.944-2115T>G
XM_017000665.1:c.944-2115T>G	XP_016856154.1:n.944-2115T>G
XR_001737042.1:n.1171+1184T>G