Canonical Allele Identifier: CA1211675
Gene: FCGR2C HGNC NCBI

Linked Data

ClinVar Variation Id: 2212289
ClinVar RCV Id: RCV004081875
dbSNP Id: rs201231731
ExAC: 1:161559384 C / G
gnomAD v2: 1-161559384-C-G
gnomAD v3: 1-161589594-C-G
gnomAD v4: 1-161589594-C-G
MyVariant Identifiers: chr1:g.161559384C>G (hg19) chr1:g.161589594C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589594C>G , CM000663.2:g.161589594C>G GRCh38
NC_000001.10:g.161559384C>G , CM000663.1:g.161559384C>G GRCh37
NC_000001.9:g.159826008C>G NCBI36
NG_011982.1:g.13256C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40563G>C ENSP00000514363.1:n.41-40563G>C
ENST00000699403.1:c.61+40774G>C ENSP00000514364.1:n.61+40774G>C
ENST00000465075.6:n.258C>G
ENST00000466542.6:c.166C>G ENSP00000426627.1:p.Pro56Ala
ENST00000473530.6:n.347C>G
ENST00000473712.6:n.188C>G
ENST00000482226.2:n.145C>G
ENST00000496692.6:n.262C>G
ENST00000502411.5:n.463C>G
ENST00000543859.5:c.166C>G ENSP00000444663.2:p.Pro56Ala
ENST00000611236.1:c.166C>G ENSP00000480953.1:p.Pro56Ala
NR_047648.1:n.265C>G
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