Canonical Allele Identifier: CA890206309

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1345931306
• gnomAD v4: 1-161589985-C-T
• MyVariant Identifiers: chr1:g.161559775C>T (hg19) ; chr1:g.161589985C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589985C>T , CM000663.2:g.161589985C>T	GRCh38
NC_000001.10:g.161559775C>T , CM000663.1:g.161559775C>T	GRCh37
NC_000001.9:g.159826399C>T	NCBI36
NG_011982.1:g.13647C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40954G>A	ENSP00000514363.1:n.41-40954G>A
ENST00000699403.1:c.61+40383G>A	ENSP00000514364.1:n.61+40383G>A
ENST00000465075.6:n.484-96C>T
ENST00000466542.6:c.391+166C>T	ENSP00000426627.1:n.391+166C>T
ENST00000473530.6:n.572+166C>T
ENST00000473712.6:n.413+166C>T
ENST00000482226.2:n.370+166C>T
ENST00000543859.5:c.388+166C>T	ENSP00000444663.2:n.388+166C>T
ENST00000611236.1:c.388+166C>T	ENSP00000480953.1:n.388+166C>T
NR_047648.1:n.490+166C>T