Canonical Allele Identifier: CA343343209

Gene: FCGR2C

Linked Data

• gnomAD v4: 1-161589805-T-C
• MyVariant Identifiers: chr1:g.161559595T>C (hg19) ; chr1:g.161589805T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161589805T>C , CM000663.2:g.161589805T>C	GRCh38
NC_000001.10:g.161559595T>C , CM000663.1:g.161559595T>C	GRCh37
NC_000001.9:g.159826219T>C	NCBI36
NG_011982.1:g.13467T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699402.1:c.41-40774A>G	ENSP00000514363.1:n.41-40774A>G
ENST00000699403.1:c.61+40563A>G	ENSP00000514364.1:n.61+40563A>G
ENST00000465075.6:n.469T>C
ENST00000466542.6:c.377T>C	ENSP00000426627.1:p.Leu126Pro
ENST00000473530.6:n.558T>C
ENST00000473712.6:n.399T>C
ENST00000482226.2:n.356T>C
ENST00000496692.6:n.473T>C
ENST00000543859.5:c.374T>C	ENSP00000444663.2:p.Leu125Pro
ENST00000611236.1:c.374T>C	ENSP00000480953.1:p.Leu125Pro
NR_047648.1:n.476T>C