Canonical Allele Identifier: CA343342792

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589757-A-G
• MyVariant Identifiers: chr1:g.161559547A>G (hg19) ; chr1:g.161589757A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589757A>G , CM000663.2:g.161589757A>G	GRCh38
NC_000001.10:g.161559547A>G , CM000663.1:g.161559547A>G	GRCh37
NC_000001.9:g.159826171A>G	NCBI36
NG_011982.1:g.13419A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40726T>C	ENSP00000514363.1:n.41-40726T>C
ENST00000699403.1:c.61+40611T>C	ENSP00000514364.1:n.61+40611T>C
ENST00000465075.6:n.421A>G
ENST00000466542.6:c.329A>G	ENSP00000426627.1:p.Glu110Gly
ENST00000473530.6:n.510A>G
ENST00000473712.6:n.351A>G
ENST00000482226.2:n.308A>G
ENST00000496692.6:n.425A>G
ENST00000543859.5:c.326A>G	ENSP00000444663.2:p.Glu109Gly
ENST00000611236.1:c.326A>G	ENSP00000480953.1:p.Glu109Gly
NR_047648.1:n.428A>G