Canonical Allele Identifier: CA1211689
Gene: FCGR2C HGNC NCBI

Linked Data

dbSNP Id: rs372812266
ExAC: 1:161559437 G / A
gnomAD v2: 1-161559437-G-A
gnomAD v3: 1-161589647-G-A
gnomAD v4: 1-161589647-G-A
MyVariant Identifiers: chr1:g.161559437G>A (hg19) chr1:g.161589647G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589647G>A , CM000663.2:g.161589647G>A GRCh38
NC_000001.10:g.161559437G>A , CM000663.1:g.161559437G>A GRCh37
NC_000001.9:g.159826061G>A NCBI36
NG_011982.1:g.13309G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40616C>T ENSP00000514363.1:n.41-40616C>T
ENST00000699403.1:c.61+40721C>T ENSP00000514364.1:n.61+40721C>T
ENST00000465075.6:n.311G>A
ENST00000466542.6:c.219G>A ENSP00000426627.1:p.Gly73=
ENST00000473530.6:n.400G>A
ENST00000473712.6:n.241G>A
ENST00000482226.2:n.198G>A
ENST00000496692.6:n.315G>A
ENST00000502411.5:n.516G>A
ENST00000543859.5:c.216G>A ENSP00000444663.2:p.Gly72=
ENST00000611236.1:c.216G>A ENSP00000480953.1:p.Gly72=
NR_047648.1:n.318G>A
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