Canonical Allele Identifier: CA343342225

Gene: FCGR2C

Linked Data

• COSMIC: COSN15624055
• MyVariant Identifiers: chr1:g.161559474C>T (hg19) ; chr1:g.161589684C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589684C>T , CM000663.2:g.161589684C>T	GRCh38
NC_000001.10:g.161559474C>T , CM000663.1:g.161559474C>T	GRCh37
NC_000001.9:g.159826098C>T	NCBI36
NG_011982.1:g.13346C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40653G>A	ENSP00000514363.1:n.41-40653G>A
ENST00000699403.1:c.61+40684G>A	ENSP00000514364.1:n.61+40684G>A
ENST00000465075.6:n.348C>T
ENST00000466542.6:c.256C>T	ENSP00000426627.1:p.His86Tyr
ENST00000473530.6:n.437C>T
ENST00000473712.6:n.278C>T
ENST00000482226.2:n.235C>T
ENST00000496692.6:n.352C>T
ENST00000502411.5:n.553C>T
ENST00000543859.5:c.253C>T	ENSP00000444663.2:p.His85Tyr
ENST00000611236.1:c.253C>T	ENSP00000480953.1:p.His85Tyr
NR_047648.1:n.355C>T