Canonical Allele Identifier: CA2320565974
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709857G= , CM000681.2:g.6709857G= GRCh38
NC_000019.9:g.6709868G= , CM000681.1:g.6709868G= GRCh37
NC_000019.8:g.6660868G= NCBI36
NG_009557.1:g.15795C= , LRG_27:g.15795C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-15C= ENSP00000512083.1:n.1564-15C=
ENST00000695654.1:c.811-15C= ENSP00000512085.1:n.811-15C=
ENST00000695655.1:c.613C= ENSP00000512086.1:n.613C=
ENST00000695692.1:n.1051-15C=
ENST00000245907.11:c.1687-15C= MANE Select ENSP00000245907.4:n.1687-15C=
ENST00000245907.10:c.1687-15C= ENSP00000245907.4:n.1687-15C=
ENST00000600763.1:n.320-15C=
NM_000064.3:c.1687-15C= NP_000055.2:n.1687-15C=
NM_000064.4:c.1687-15C= MANE Select NP_000055.2:n.1687-15C=
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