Canonical Allele Identifier: CA343342002

Gene: FCGR2C

Linked Data

• MyVariant Identifiers: chr1:g.161559436G>C (hg19) ; chr1:g.161589646G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589646G>C , CM000663.2:g.161589646G>C	GRCh38
NC_000001.10:g.161559436G>C , CM000663.1:g.161559436G>C	GRCh37
NC_000001.9:g.159826060G>C	NCBI36
NG_011982.1:g.13308G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40615C>G	ENSP00000514363.1:n.41-40615C>G
ENST00000699403.1:c.61+40722C>G	ENSP00000514364.1:n.61+40722C>G
ENST00000465075.6:n.310G>C
ENST00000466542.6:c.218G>C	ENSP00000426627.1:p.Gly73Ala
ENST00000473530.6:n.399G>C
ENST00000473712.6:n.240G>C
ENST00000482226.2:n.197G>C
ENST00000496692.6:n.314G>C
ENST00000502411.5:n.515G>C
ENST00000543859.5:c.215G>C	ENSP00000444663.2:p.Gly72Ala
ENST00000611236.1:c.215G>C	ENSP00000480953.1:p.Gly72Ala
NR_047648.1:n.317G>C