Canonical Allele Identifier: CA1211684

Gene: FCGR2C

Linked Data

• dbSNP Id: rs760731369
• ExAC: 1:161559412 A / C
• gnomAD v2: 1-161559412-A-C
• MyVariant Identifiers: chr1:g.161559412A>C (hg19) ; chr1:g.161589622A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589622A>C , CM000663.2:g.161589622A>C	GRCh38
NC_000001.10:g.161559412A>C , CM000663.1:g.161559412A>C	GRCh37
NC_000001.9:g.159826036A>C	NCBI36
NG_011982.1:g.13284A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40591T>G	ENSP00000514363.1:n.41-40591T>G
ENST00000699403.1:c.61+40746T>G	ENSP00000514364.1:n.61+40746T>G
ENST00000465075.6:n.286A>C
ENST00000466542.6:c.194A>C	ENSP00000426627.1:p.Asp65Ala
ENST00000473530.6:n.375A>C
ENST00000473712.6:n.216A>C
ENST00000482226.2:n.173A>C
ENST00000496692.6:n.290A>C
ENST00000502411.5:n.491A>C
ENST00000543859.5:c.191A>C	ENSP00000444663.2:p.Asp64Ala
ENST00000611236.1:c.191A>C	ENSP00000480953.1:p.Asp64Ala
NR_047648.1:n.293A>C