Canonical Allele Identifier: CA343342362

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559500C>A (hg19) ; chr1:g.161589710C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589710C>A , CM000663.2:g.161589710C>A	GRCh38
NC_000001.10:g.161559500C>A , CM000663.1:g.161559500C>A	GRCh37
NC_000001.9:g.159826124C>A	NCBI36
NG_011982.1:g.13372C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40679G>T	ENSP00000514363.1:n.41-40679G>T
ENST00000699403.1:c.61+40658G>T	ENSP00000514364.1:n.61+40658G>T
ENST00000465075.6:n.374C>A
ENST00000466542.6:c.282C>A	ENSP00000426627.1:p.His94Gln
ENST00000473530.6:n.463C>A
ENST00000473712.6:n.304C>A
ENST00000482226.2:n.261C>A
ENST00000496692.6:n.378C>A
ENST00000543859.5:c.279C>A	ENSP00000444663.2:p.His93Gln
ENST00000611236.1:c.279C>A	ENSP00000480953.1:p.His93Gln
NR_047648.1:n.381C>A