Canonical Allele Identifier: CA1211693

Gene: FCGR2C

Linked Data

• dbSNP Id: rs746714007
• ExAC: 1:161559454 G / A
• gnomAD v2: 1-161559454-G-A
• gnomAD v4: 1-161589664-G-A
• MyVariant Identifiers: chr1:g.161559454G>A (hg19) ; chr1:g.161589664G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589664G>A , CM000663.2:g.161589664G>A	GRCh38
NC_000001.10:g.161559454G>A , CM000663.1:g.161559454G>A	GRCh37
NC_000001.9:g.159826078G>A	NCBI36
NG_011982.1:g.13326G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40633C>T	ENSP00000514363.1:n.41-40633C>T
ENST00000699403.1:c.61+40704C>T	ENSP00000514364.1:n.61+40704C>T
ENST00000465075.6:n.328G>A
ENST00000466542.6:c.236G>A	ENSP00000426627.1:p.Ser79Asn
ENST00000473530.6:n.417G>A
ENST00000473712.6:n.258G>A
ENST00000482226.2:n.215G>A
ENST00000496692.6:n.332G>A
ENST00000502411.5:n.533G>A
ENST00000543859.5:c.233G>A	ENSP00000444663.2:p.Ser78Asn
ENST00000611236.1:c.233G>A	ENSP00000480953.1:p.Ser78Asn
NR_047648.1:n.335G>A