Canonical Allele Identifier: CA1211718
Gene: FCGR2C HGNC NCBI

Linked Data

dbSNP Id: rs138747765
ExAC: 1:161559571 C / T
gnomAD v2: 1-161559571-C-T
gnomAD v3: 1-161589781-C-T
gnomAD v4: 1-161589781-C-T
MyVariant Identifiers: chr1:g.161559571C>T (hg19) chr1:g.161589781C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589781C>T , CM000663.2:g.161589781C>T GRCh38
NC_000001.10:g.161559571C>T , CM000663.1:g.161559571C>T GRCh37
NC_000001.9:g.159826195C>T NCBI36
NG_011982.1:g.13443C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000699402.1:c.41-40750G>A ENSP00000514363.1:n.41-40750G>A
ENST00000699403.1:c.61+40587G>A ENSP00000514364.1:n.61+40587G>A
ENST00000465075.6:n.445C>T
ENST00000466542.6:c.353C>T ENSP00000426627.1:p.Thr118Ile
ENST00000473530.6:n.534C>T
ENST00000473712.6:n.375C>T
ENST00000482226.2:n.332C>T
ENST00000496692.6:n.449C>T
ENST00000543859.5:c.350C>T ENSP00000444663.2:p.Thr117Ile
ENST00000611236.1:c.350C>T ENSP00000480953.1:p.Thr117Ile
NR_047648.1:n.452C>T
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