Canonical Allele Identifier: CA1211677
Gene: FCGR2C HGNC NCBI

Linked Data

dbSNP Id: rs759550223
ExAC: 1:161559387 T / C
gnomAD v2: 1-161559387-T-C
gnomAD v3: 1-161589597-T-C
gnomAD v4: 1-161589597-T-C
COSMIC: COSN9457166 COSN18959613 COSN18959615 COSN18959617
MyVariant Identifiers: chr1:g.161559387T>C (hg19) chr1:g.161589597T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589597T>C , CM000663.2:g.161589597T>C GRCh38
NC_000001.10:g.161559387T>C , CM000663.1:g.161559387T>C GRCh37
NC_000001.9:g.159826011T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40566A>G ENSP00000514363.1:n.41-40566A>G
ENST00000699403.1:c.61+40771A>G ENSP00000514364.1:n.61+40771A>G
ENST00000465075.6:n.261T>C
ENST00000466542.6:c.169T>C ENSP00000426627.1:p.Ter57Gln
ENST00000473530.6:n.350T>C
ENST00000473712.6:n.191T>C
ENST00000482226.2:n.148T>C
ENST00000496692.6:n.265T>C
ENST00000502411.5:n.466T>C
ENST00000543859.5:c.168+1T>C ENSP00000444663.2:n.168+1T>C
ENST00000611236.1:c.168+1T>C ENSP00000480953.1:n.168+1T>C
NR_047648.1:n.268T>C
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