Canonical Allele Identifier: CA2648792112
Gene: FCGR2C HGNC NCBI

Linked Data

gnomAD v4: 1-161589969-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589969C>A , CM000663.2:g.161589969C>A GRCh38
NC_000001.10:g.161559759C>A , CM000663.1:g.161559759C>A GRCh37
NC_000001.9:g.159826383C>A NCBI36
NG_011982.1:g.13631C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40938G>T ENSP00000514363.1:n.41-40938G>T
ENST00000699403.1:c.61+40399G>T ENSP00000514364.1:n.61+40399G>T
ENST00000465075.6:n.484-112C>A
ENST00000466542.6:c.391+150C>A ENSP00000426627.1:n.391+150C>A
ENST00000473530.6:n.572+150C>A
ENST00000473712.6:n.413+150C>A
ENST00000482226.2:n.370+150C>A
ENST00000543859.5:c.388+150C>A ENSP00000444663.2:n.388+150C>A
ENST00000611236.1:c.388+150C>A ENSP00000480953.1:n.388+150C>A
NR_047648.1:n.490+150C>A
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