Canonical Allele Identifier: CA1211725

Gene: FCGR2C

Linked Data

• dbSNP Id: rs773015724
• ExAC: 1:161559592 A / C
• gnomAD v2: 1-161559592-A-C
• gnomAD v4: 1-161589802-A-C
• MyVariant Identifiers: chr1:g.161559592A>C (hg19) ; chr1:g.161589802A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589802A>C , CM000663.2:g.161589802A>C	GRCh38
NC_000001.10:g.161559592A>C , CM000663.1:g.161559592A>C	GRCh37
NC_000001.9:g.159826216A>C	NCBI36
NG_011982.1:g.13464A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40771T>G	ENSP00000514363.1:n.41-40771T>G
ENST00000699403.1:c.61+40566T>G	ENSP00000514364.1:n.61+40566T>G
ENST00000465075.6:n.466A>C
ENST00000466542.6:c.374A>C	ENSP00000426627.1:p.His125Pro
ENST00000473530.6:n.555A>C
ENST00000473712.6:n.396A>C
ENST00000482226.2:n.353A>C
ENST00000496692.6:n.470A>C
ENST00000543859.5:c.371A>C	ENSP00000444663.2:p.His124Pro
ENST00000611236.1:c.371A>C	ENSP00000480953.1:p.His124Pro
NR_047648.1:n.473A>C