Canonical Allele Identifier: CA343343243

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589810-G-C
• MyVariant Identifiers: chr1:g.161559600G>C (hg19) ; chr1:g.161589810G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589810G>C , CM000663.2:g.161589810G>C	GRCh38
NC_000001.10:g.161559600G>C , CM000663.1:g.161559600G>C	GRCh37
NC_000001.9:g.159826224G>C	NCBI36
NG_011982.1:g.13472G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40779C>G	ENSP00000514363.1:n.41-40779C>G
ENST00000699403.1:c.61+40558C>G	ENSP00000514364.1:n.61+40558C>G
ENST00000465075.6:n.474G>C
ENST00000466542.6:c.382G>C	ENSP00000426627.1:p.Val128Leu
ENST00000473530.6:n.563G>C
ENST00000473712.6:n.404G>C
ENST00000482226.2:n.361G>C
ENST00000496692.6:n.478G>C
ENST00000543859.5:c.379G>C	ENSP00000444663.2:p.Val127Leu
ENST00000611236.1:c.379G>C	ENSP00000480953.1:p.Val127Leu
NR_047648.1:n.481G>C