Canonical Allele Identifier: CA2320559051

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697416C= , CM000681.2:g.6697416C=	GRCh38
NC_000019.9:g.6697427C= , CM000681.1:g.6697427C=	GRCh37
NC_000019.8:g.6648427C=	NCBI36
NG_009557.1:g.28236G= , LRG_27:g.28236G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1072G=
ENST00000695652.1:c.2601G=	ENSP00000512083.1:p.Gln867=
ENST00000695653.1:c.633G=	ENSP00000512084.1:p.Gln211=
ENST00000695654.1:c.1848G=	ENSP00000512085.1:p.Gln616=
ENST00000695655.1:c.1665G=	ENSP00000512086.1:n.1665G=
ENST00000695692.1:n.2088G=
ENST00000245907.11:c.2724G= MANE Select	ENSP00000245907.4:p.Gln908=
ENST00000245907.10:c.2724G=	ENSP00000245907.4:p.Gln908=
ENST00000594005.1:n.300G=
NM_000064.3:c.2724G=	NP_000055.2:p.Gln908=
NM_000064.4:c.2724G= MANE Select	NP_000055.2:p.Gln908=