Canonical Allele Identifier: CA343342099

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589663-A-C
• MyVariant Identifiers: chr1:g.161559453A>C (hg19) ; chr1:g.161589663A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589663A>C , CM000663.2:g.161589663A>C	GRCh38
NC_000001.10:g.161559453A>C , CM000663.1:g.161559453A>C	GRCh37
NC_000001.9:g.159826077A>C	NCBI36
NG_011982.1:g.13325A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40632T>G	ENSP00000514363.1:n.41-40632T>G
ENST00000699403.1:c.61+40705T>G	ENSP00000514364.1:n.61+40705T>G
ENST00000465075.6:n.327A>C
ENST00000466542.6:c.235A>C	ENSP00000426627.1:p.Ser79Arg
ENST00000473530.6:n.416A>C
ENST00000473712.6:n.257A>C
ENST00000482226.2:n.214A>C
ENST00000496692.6:n.331A>C
ENST00000502411.5:n.532A>C
ENST00000543859.5:c.232A>C	ENSP00000444663.2:p.Ser78Arg
ENST00000611236.1:c.232A>C	ENSP00000480953.1:p.Ser78Arg
NR_047648.1:n.334A>C