Canonical Allele Identifier: CA343342337

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559493C>T (hg19) ; chr1:g.161589703C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589703C>T , CM000663.2:g.161589703C>T	GRCh38
NC_000001.10:g.161559493C>T , CM000663.1:g.161559493C>T	GRCh37
NC_000001.9:g.159826117C>T	NCBI36
NG_011982.1:g.13365C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40672G>A	ENSP00000514363.1:n.41-40672G>A
ENST00000699403.1:c.61+40665G>A	ENSP00000514364.1:n.61+40665G>A
ENST00000465075.6:n.367C>T
ENST00000466542.6:c.275C>T	ENSP00000426627.1:p.Pro92Leu
ENST00000473530.6:n.456C>T
ENST00000473712.6:n.297C>T
ENST00000482226.2:n.254C>T
ENST00000496692.6:n.371C>T
ENST00000543859.5:c.272C>T	ENSP00000444663.2:p.Pro91Leu
ENST00000611236.1:c.272C>T	ENSP00000480953.1:p.Pro91Leu
NR_047648.1:n.374C>T