Canonical Allele Identifier: CA2320567694
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6712878T= , CM000681.2:g.6712878T= GRCh38
NC_000019.9:g.6712889T= , CM000681.1:g.6712889T= GRCh37
NC_000019.8:g.6663889T= NCBI36
NG_009557.1:g.12774A= , LRG_27:g.12774A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.881-255A= ENSP00000512083.1:n.881-255A=
ENST00000695654.1:c.128-255A= ENSP00000512085.1:n.128-255A=
ENST00000695692.1:n.328-215A=
ENST00000245907.11:c.1004-255A= MANE Select ENSP00000245907.4:n.1004-255A=
ENST00000245907.10:c.1004-255A= ENSP00000245907.4:n.1004-255A=
ENST00000594270.5:n.128-276A=
ENST00000595577.1:n.508-255A=
ENST00000597442.5:n.254-255A=
NM_000064.3:c.1004-255A= NP_000055.2:n.1004-255A=
NM_000064.4:c.1004-255A= MANE Select NP_000055.2:n.1004-255A=
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