Canonical Allele Identifier: CA343341914

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559421C>A (hg19) ; chr1:g.161589631C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589631C>A , CM000663.2:g.161589631C>A	GRCh38
NC_000001.10:g.161559421C>A , CM000663.1:g.161559421C>A	GRCh37
NC_000001.9:g.159826045C>A	NCBI36
NG_011982.1:g.13293C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40600G>T	ENSP00000514363.1:n.41-40600G>T
ENST00000699403.1:c.61+40737G>T	ENSP00000514364.1:n.61+40737G>T
ENST00000465075.6:n.295C>A
ENST00000466542.6:c.203C>A	ENSP00000426627.1:p.Thr68Asn
ENST00000473530.6:n.384C>A
ENST00000473712.6:n.225C>A
ENST00000482226.2:n.182C>A
ENST00000496692.6:n.299C>A
ENST00000502411.5:n.500C>A
ENST00000543859.5:c.200C>A	ENSP00000444663.2:p.Thr67Asn
ENST00000611236.1:c.200C>A	ENSP00000480953.1:p.Thr67Asn
NR_047648.1:n.302C>A