Canonical Allele Identifier: CA1211691

Gene: FCGR2C

Linked Data

• dbSNP Id: rs758002521
• ExAC: 1:161559443 C / A
• gnomAD v2: 1-161559443-C-A
• gnomAD v4: 1-161589653-C-A
• MyVariant Identifiers: chr1:g.161559443C>A (hg19) ; chr1:g.161589653C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589653C>A , CM000663.2:g.161589653C>A	GRCh38
NC_000001.10:g.161559443C>A , CM000663.1:g.161559443C>A	GRCh37
NC_000001.9:g.159826067C>A	NCBI36
NG_011982.1:g.13315C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40622G>T	ENSP00000514363.1:n.41-40622G>T
ENST00000699403.1:c.61+40715G>T	ENSP00000514364.1:n.61+40715G>T
ENST00000465075.6:n.317C>A
ENST00000466542.6:c.225C>A	ENSP00000426627.1:p.His75Gln
ENST00000473530.6:n.406C>A
ENST00000473712.6:n.247C>A
ENST00000482226.2:n.204C>A
ENST00000496692.6:n.321C>A
ENST00000502411.5:n.522C>A
ENST00000543859.5:c.222C>A	ENSP00000444663.2:p.His74Gln
ENST00000611236.1:c.222C>A	ENSP00000480953.1:p.His74Gln
NR_047648.1:n.324C>A