Canonical Allele Identifier: CA31691002

Gene: FCGR2A

Linked Data

• dbSNP Id: rs511278
• gnomAD v2: 1-161490896-T-C
• gnomAD v3: 1-161521106-T-C
• gnomAD v4: 1-161521106-T-C
• MyVariant Identifiers: chr1:g.161490896T>C (hg19) ; chr1:g.161521106T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161521106T>C , CM000663.2:g.161521106T>C	GRCh38
NC_000001.10:g.161490896T>C , CM000663.1:g.161490896T>C	GRCh37
NC_000001.9:g.159757520T>C	NCBI36
NG_012066.1:g.20692T>C
NG_012066.2:g.20692T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000467525.5:c.918+1393T>C	ENSP00000476495.1:n.918+1393T>C
ENST00000491841.1:n.425+1115T>C
XM_011509287.1:c.*23+1115T>C	XP_011507589.1:n.*23+1115T>C
XM_011509288.1:c.*23+1115T>C	XP_011507590.1:n.*23+1115T>C
XM_011509289.1:c.*23+1115T>C	XP_011507591.1:n.*23+1115T>C
XM_011509287.2:c.*23+1115T>C	XP_011507589.1:n.*23+1115T>C
XM_017000664.1:c.944-2184T>C	XP_016856153.1:n.944-2184T>C
XM_017000665.1:c.944-2184T>C	XP_016856154.1:n.944-2184T>C
XR_001737042.1:n.1171+1115T>C