Canonical Allele Identifier: CA890220244
Gene: FCGR2A HGNC NCBI

Linked Data

dbSNP Id: rs511278
MyVariant Identifiers: chr1:g.161490896T>A (hg19) chr1:g.161521106T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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