Canonical Allele Identifier: CA421417459
Gene: FCGR2C HGNC NCBI

Linked Data

gnomAD v4: 1-161589833-G-A
MyVariant Identifiers: chr1:g.161559623G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589833G>A , CM000663.2:g.161589833G>A GRCh38
NC_000001.10:g.161559623G>A , CM000663.1:g.161559623G>A GRCh37
NC_000001.9:g.159826247G>A NCBI36
NG_011982.1:g.13495G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40802C>T ENSP00000514363.1:n.41-40802C>T
ENST00000699403.1:c.61+40535C>T ENSP00000514364.1:n.61+40535C>T
ENST00000465075.6:n.483+14G>A
ENST00000466542.6:c.391+14G>A ENSP00000426627.1:n.391+14G>A
ENST00000473530.6:n.572+14G>A
ENST00000473712.6:n.413+14G>A
ENST00000482226.2:n.370+14G>A
ENST00000496692.6:n.501G>A
ENST00000543859.5:c.388+14G>A ENSP00000444663.2:n.388+14G>A
ENST00000611236.1:c.388+14G>A ENSP00000480953.1:n.388+14G>A
NR_047648.1:n.490+14G>A
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