Canonical Allele Identifier: CA2320567682
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6712849C= , CM000681.2:g.6712849C= GRCh38
NC_000019.9:g.6712860C= , CM000681.1:g.6712860C= GRCh37
NC_000019.8:g.6663860C= NCBI36
NG_009557.1:g.12803G= , LRG_27:g.12803G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.881-226G= ENSP00000512083.1:n.881-226G=
ENST00000695654.1:c.128-226G= ENSP00000512085.1:n.128-226G=
ENST00000695692.1:n.328-186G=
ENST00000245907.11:c.1004-226G= MANE Select ENSP00000245907.4:n.1004-226G=
ENST00000245907.10:c.1004-226G= ENSP00000245907.4:n.1004-226G=
ENST00000594270.5:n.128-247G=
ENST00000595577.1:n.508-226G=
ENST00000597442.5:n.254-226G=
NM_000064.3:c.1004-226G= NP_000055.2:n.1004-226G=
NM_000064.4:c.1004-226G= MANE Select NP_000055.2:n.1004-226G=
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