Canonical Allele Identifier: CA1211685
Gene: FCGR2C HGNC NCBI

Linked Data

dbSNP Id: rs535169151
ExAC: 1:161559429 T / C
gnomAD v2: 1-161559429-T-C
gnomAD v3: 1-161589639-T-C
gnomAD v4: 1-161589639-T-C
MyVariant Identifiers: chr1:g.161559429T>C (hg19) chr1:g.161589639T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589639T>C , CM000663.2:g.161589639T>C GRCh38
NC_000001.10:g.161559429T>C , CM000663.1:g.161559429T>C GRCh37
NC_000001.9:g.159826053T>C NCBI36
NG_011982.1:g.13301T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40608A>G ENSP00000514363.1:n.41-40608A>G
ENST00000699403.1:c.61+40729A>G ENSP00000514364.1:n.61+40729A>G
ENST00000465075.6:n.303T>C
ENST00000466542.6:c.211T>C ENSP00000426627.1:p.Cys71Arg
ENST00000473530.6:n.392T>C
ENST00000473712.6:n.233T>C
ENST00000482226.2:n.190T>C
ENST00000496692.6:n.307T>C
ENST00000502411.5:n.508T>C
ENST00000543859.5:c.208T>C ENSP00000444663.2:p.Cys70Arg
ENST00000611236.1:c.208T>C ENSP00000480953.1:p.Cys70Arg
NR_047648.1:n.310T>C
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