Canonical Allele Identifier: CA421417441

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559605T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589815T>C , CM000663.2:g.161589815T>C	GRCh38
NC_000001.10:g.161559605T>C , CM000663.1:g.161559605T>C	GRCh37
NC_000001.9:g.159826229T>C	NCBI36
NG_011982.1:g.13477T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40784A>G	ENSP00000514363.1:n.41-40784A>G
ENST00000699403.1:c.61+40553A>G	ENSP00000514364.1:n.61+40553A>G
ENST00000465075.6:n.479T>C
ENST00000466542.6:c.387T>C	ENSP00000426627.1:p.Leu129=
ENST00000473530.6:n.568T>C
ENST00000473712.6:n.409T>C
ENST00000482226.2:n.366T>C
ENST00000496692.6:n.483T>C
ENST00000543859.5:c.384T>C	ENSP00000444663.2:p.Leu128=
ENST00000611236.1:c.384T>C	ENSP00000480953.1:p.Leu128=
NR_047648.1:n.486T>C