Canonical Allele Identifier: CA2320567726
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6712973G= , CM000681.2:g.6712973G= GRCh38
NC_000019.9:g.6712984G= , CM000681.1:g.6712984G= GRCh37
NC_000019.8:g.6663984G= NCBI36
NG_009557.1:g.12679C= , LRG_27:g.12679C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.880+216C= ENSP00000512083.1:n.880+216C=
ENST00000695654.1:c.127+216C= ENSP00000512085.1:n.127+216C=
ENST00000695692.1:n.327+216C=
ENST00000245907.11:c.1003+216C= MANE Select ENSP00000245907.4:n.1003+216C=
ENST00000245907.10:c.1003+216C= ENSP00000245907.4:n.1003+216C=
ENST00000594270.5:n.127+216C=
ENST00000595577.1:n.507+216C=
ENST00000597442.5:n.253+216C=
NM_000064.3:c.1003+216C= NP_000055.2:n.1003+216C=
NM_000064.4:c.1003+216C= MANE Select NP_000055.2:n.1003+216C=
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