Canonical Allele Identifier: CA890206311
Gene: FCGR2C HGNC NCBI

Linked Data

dbSNP Id: rs1431633001
gnomAD v3: 1-161589987-G-C
gnomAD v4: 1-161589987-G-C
MyVariant Identifiers: chr1:g.161559777G>C (hg19) chr1:g.161589987G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589987G>C , CM000663.2:g.161589987G>C GRCh38
NC_000001.10:g.161559777G>C , CM000663.1:g.161559777G>C GRCh37
NC_000001.9:g.159826401G>C NCBI36
NG_011982.1:g.13649G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40956C>G ENSP00000514363.1:n.41-40956C>G
ENST00000699403.1:c.61+40381C>G ENSP00000514364.1:n.61+40381C>G
ENST00000465075.6:n.484-94G>C
ENST00000466542.6:c.391+168G>C ENSP00000426627.1:n.391+168G>C
ENST00000473530.6:n.572+168G>C
ENST00000473712.6:n.413+168G>C
ENST00000482226.2:n.370+168G>C
ENST00000543859.5:c.388+168G>C ENSP00000444663.2:n.388+168G>C
ENST00000611236.1:c.388+168G>C ENSP00000480953.1:n.388+168G>C
NR_047648.1:n.490+168G>C
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