Canonical Allele Identifier: CA890206285

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1488251187
• gnomAD v3: 1-161589925-G-A
• gnomAD v4: 1-161589925-G-A
• MyVariant Identifiers: chr1:g.161559715G>A (hg19) ; chr1:g.161589925G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589925G>A , CM000663.2:g.161589925G>A	GRCh38
NC_000001.10:g.161559715G>A , CM000663.1:g.161559715G>A	GRCh37
NC_000001.9:g.159826339G>A	NCBI36
NG_011982.1:g.13587G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40894C>T	ENSP00000514363.1:n.41-40894C>T
ENST00000699403.1:c.61+40443C>T	ENSP00000514364.1:n.61+40443C>T
ENST00000465075.6:n.483+106G>A
ENST00000466542.6:c.391+106G>A	ENSP00000426627.1:n.391+106G>A
ENST00000473530.6:n.572+106G>A
ENST00000473712.6:n.413+106G>A
ENST00000482226.2:n.370+106G>A
ENST00000543859.5:c.388+106G>A	ENSP00000444663.2:n.388+106G>A
ENST00000611236.1:c.388+106G>A	ENSP00000480953.1:n.388+106G>A
NR_047648.1:n.490+106G>A