Canonical Allele Identifier: CA2320567764
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713058C= , CM000681.2:g.6713058C= GRCh38
NC_000019.9:g.6713069C= , CM000681.1:g.6713069C= GRCh37
NC_000019.8:g.6664069C= NCBI36
NG_009557.1:g.12594G= , LRG_27:g.12594G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.880+131G= ENSP00000512083.1:n.880+131G=
ENST00000695654.1:c.127+131G= ENSP00000512085.1:n.127+131G=
ENST00000695692.1:n.327+131G=
ENST00000245907.11:c.1003+131G= MANE Select ENSP00000245907.4:n.1003+131G=
ENST00000245907.10:c.1003+131G= ENSP00000245907.4:n.1003+131G=
ENST00000594270.5:n.127+131G=
ENST00000595577.1:n.507+131G=
ENST00000597442.5:n.253+131G=
NM_000064.3:c.1003+131G= NP_000055.2:n.1003+131G=
NM_000064.4:c.1003+131G= MANE Select NP_000055.2:n.1003+131G=
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