Canonical Allele Identifier: CA2320559035

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697350C= , CM000681.2:g.6697350C=	GRCh38
NC_000019.9:g.6697361C= , CM000681.1:g.6697361C=	GRCh37
NC_000019.8:g.6648361C=	NCBI36
NG_009557.1:g.28302G= , LRG_27:g.28302G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1138G=
ENST00000695652.1:c.2667G=	ENSP00000512083.1:p.Lys889=
ENST00000695653.1:c.699G=	ENSP00000512084.1:p.Lys233=
ENST00000695654.1:c.1914G=	ENSP00000512085.1:p.Lys638=
ENST00000695655.1:c.1731G=	ENSP00000512086.1:n.1731G=
ENST00000695692.1:n.2154G=
ENST00000245907.11:c.2790G= MANE Select	ENSP00000245907.4:p.Lys930=
ENST00000245907.10:c.2790G=	ENSP00000245907.4:p.Lys930=
ENST00000594005.1:n.366G=
NM_000064.3:c.2790G=	NP_000055.2:p.Lys930=
NM_000064.4:c.2790G= MANE Select	NP_000055.2:p.Lys930=