Canonical Allele Identifier: CA421417482

Gene: FCGR2C

Linked Data

• dbSNP Id: rs1678465758
• gnomAD v4: 1-161589841-G-C
• MyVariant Identifiers: chr1:g.161559631G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589841G>C , CM000663.2:g.161589841G>C	GRCh38
NC_000001.10:g.161559631G>C , CM000663.1:g.161559631G>C	GRCh37
NC_000001.9:g.159826255G>C	NCBI36
NG_011982.1:g.13503G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40810C>G	ENSP00000514363.1:n.41-40810C>G
ENST00000699403.1:c.61+40527C>G	ENSP00000514364.1:n.61+40527C>G
ENST00000465075.6:n.483+22G>C
ENST00000466542.6:c.391+22G>C	ENSP00000426627.1:n.391+22G>C
ENST00000473530.6:n.572+22G>C
ENST00000473712.6:n.413+22G>C
ENST00000482226.2:n.370+22G>C
ENST00000496692.6:n.509G>C
ENST00000543859.5:c.388+22G>C	ENSP00000444663.2:n.388+22G>C
ENST00000611236.1:c.388+22G>C	ENSP00000480953.1:n.388+22G>C
NR_047648.1:n.490+22G>C