Canonical Allele Identifier: CA1211723

Gene: FCGR2C

Linked Data

• dbSNP Id: rs761811775
• ExAC: 1:161559582 G / A
• gnomAD v2: 1-161559582-G-A
• gnomAD v4: 1-161589792-G-A
• COSMIC: COSN20089612
• MyVariant Identifiers: chr1:g.161559582G>A (hg19) ; chr1:g.161589792G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589792G>A , CM000663.2:g.161589792G>A	GRCh38
NC_000001.10:g.161559582G>A , CM000663.1:g.161559582G>A	GRCh37
NC_000001.9:g.159826206G>A	NCBI36
NG_011982.1:g.13454G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40761C>T	ENSP00000514363.1:n.41-40761C>T
ENST00000699403.1:c.61+40576C>T	ENSP00000514364.1:n.61+40576C>T
ENST00000465075.6:n.456G>A
ENST00000466542.6:c.364G>A	ENSP00000426627.1:p.Asp122Asn
ENST00000473530.6:n.545G>A
ENST00000473712.6:n.386G>A
ENST00000482226.2:n.343G>A
ENST00000496692.6:n.460G>A
ENST00000543859.5:c.361G>A	ENSP00000444663.2:p.Asp121Asn
ENST00000611236.1:c.361G>A	ENSP00000480953.1:p.Asp121Asn
NR_047648.1:n.463G>A