Canonical Allele Identifier: CA2320567773
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713073C= , CM000681.2:g.6713073C= GRCh38
NC_000019.9:g.6713084C= , CM000681.1:g.6713084C= GRCh37
NC_000019.8:g.6664084C= NCBI36
NG_009557.1:g.12579G= , LRG_27:g.12579G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.880+116G= ENSP00000512083.1:n.880+116G=
ENST00000695654.1:c.127+116G= ENSP00000512085.1:n.127+116G=
ENST00000695692.1:n.327+116G=
ENST00000245907.11:c.1003+116G= MANE Select ENSP00000245907.4:n.1003+116G=
ENST00000245907.10:c.1003+116G= ENSP00000245907.4:n.1003+116G=
ENST00000594270.5:n.127+116G=
ENST00000595577.1:n.507+116G=
ENST00000597442.5:n.253+116G=
NM_000064.3:c.1003+116G= NP_000055.2:n.1003+116G=
NM_000064.4:c.1003+116G= MANE Select NP_000055.2:n.1003+116G=
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