Canonical Allele Identifier: CA2320565854
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709615A= , CM000681.2:g.6709615A= GRCh38
NC_000019.9:g.6709626A= , CM000681.1:g.6709626A= GRCh37
NC_000019.8:g.6660626A= NCBI36
NG_009557.1:g.16037T= , LRG_27:g.16037T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1722+69T= ENSP00000512083.1:n.1722+69T=
ENST00000695654.1:c.969+69T= ENSP00000512085.1:n.969+69T=
ENST00000695655.1:c.786+69T= ENSP00000512086.1:n.786+69T=
ENST00000695692.1:n.1209+69T=
ENST00000245907.11:c.1845+69T= MANE Select ENSP00000245907.4:n.1845+69T=
ENST00000245907.10:c.1845+69T= ENSP00000245907.4:n.1845+69T=
NM_000064.3:c.1845+69T= NP_000055.2:n.1845+69T=
NM_000064.4:c.1845+69T= MANE Select NP_000055.2:n.1845+69T=
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