Canonical Allele Identifier: CA2320568001
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713596G= , CM000681.2:g.6713596G= GRCh38
NC_000019.9:g.6713607G= , CM000681.1:g.6713607G= GRCh37
NC_000019.8:g.6664607G= NCBI36
NG_009557.1:g.12056C= , LRG_27:g.12056C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-87C= ENSP00000512083.1:n.651-87C=
ENST00000695692.1:n.11C=
ENST00000245907.11:c.774-87C= MANE Select ENSP00000245907.4:n.774-87C=
ENST00000245907.10:c.774-87C= ENSP00000245907.4:n.774-87C=
ENST00000595577.1:n.278-87C=
ENST00000597442.5:n.24-87C=
NM_000064.3:c.774-87C= NP_000055.2:n.774-87C=
NM_000064.4:c.774-87C= MANE Select NP_000055.2:n.774-87C=
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