Canonical Allele Identifier: CA343341709

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1381773491
• gnomAD v2: 1-161559383-G-T
• gnomAD v3: 1-161589593-G-T
• gnomAD v4: 1-161589593-G-T
• MyVariant Identifiers: chr1:g.161559383G>T (hg19) ; chr1:g.161589593G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589593G>T , CM000663.2:g.161589593G>T	GRCh38
NC_000001.10:g.161559383G>T , CM000663.1:g.161559383G>T	GRCh37
NC_000001.9:g.159826007G>T	NCBI36
NG_011982.1:g.13255G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40562C>A	ENSP00000514363.1:n.41-40562C>A
ENST00000699403.1:c.61+40775C>A	ENSP00000514364.1:n.61+40775C>A
ENST00000465075.6:n.257G>T
ENST00000466542.6:c.165G>T	ENSP00000426627.1:p.Glu55Asp
ENST00000473530.6:n.346G>T
ENST00000473712.6:n.187G>T
ENST00000482226.2:n.144G>T
ENST00000496692.6:n.261G>T
ENST00000502411.5:n.462G>T
ENST00000543859.5:c.165G>T	ENSP00000444663.2:p.Glu55Asp
ENST00000611236.1:c.165G>T	ENSP00000480953.1:p.Glu55Asp
NR_047648.1:n.264G>T