Canonical Allele Identifier: CA421417182

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559380C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589590C>A , CM000663.2:g.161589590C>A	GRCh38
NC_000001.10:g.161559380C>A , CM000663.1:g.161559380C>A	GRCh37
NC_000001.9:g.159826004C>A	NCBI36
NG_011982.1:g.13252C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40559G>T	ENSP00000514363.1:n.41-40559G>T
ENST00000699403.1:c.61+40778G>T	ENSP00000514364.1:n.61+40778G>T
ENST00000465075.6:n.254C>A
ENST00000466542.6:c.162C>A	ENSP00000426627.1:p.Leu54=
ENST00000473530.6:n.343C>A
ENST00000473712.6:n.184C>A
ENST00000482226.2:n.141C>A
ENST00000496692.6:n.258C>A
ENST00000502411.5:n.459C>A
ENST00000543859.5:c.162C>A	ENSP00000444663.2:p.Leu54=
ENST00000611236.1:c.162C>A	ENSP00000480953.1:p.Leu54=
NR_047648.1:n.261C>A