Canonical Allele Identifier: CA421417439
Gene: FCGR2C HGNC NCBI

Linked Data

dbSNP Id: rs1325679991
gnomAD v2: 1-161559602-G-T
gnomAD v3: 1-161589812-G-T
gnomAD v4: 1-161589812-G-T
MyVariant Identifiers: chr1:g.161559602G>T (hg19) chr1:g.161589812G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589812G>T , CM000663.2:g.161589812G>T GRCh38
NC_000001.10:g.161559602G>T , CM000663.1:g.161559602G>T GRCh37
NC_000001.9:g.159826226G>T NCBI36
NG_011982.1:g.13474G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40781C>A ENSP00000514363.1:n.41-40781C>A
ENST00000699403.1:c.61+40556C>A ENSP00000514364.1:n.61+40556C>A
ENST00000465075.6:n.476G>T
ENST00000466542.6:c.384G>T ENSP00000426627.1:p.Val128=
ENST00000473530.6:n.565G>T
ENST00000473712.6:n.406G>T
ENST00000482226.2:n.363G>T
ENST00000496692.6:n.480G>T
ENST00000543859.5:c.381G>T ENSP00000444663.2:p.Val127=
ENST00000611236.1:c.381G>T ENSP00000480953.1:p.Val127=
NR_047648.1:n.483G>T
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