Canonical Allele Identifier: CA2320553466

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686201C= , CM000681.2:g.6686201C=	GRCh38
NC_000019.9:g.6686212C= , CM000681.1:g.6686212C=	GRCh37
NC_000019.8:g.6637212C=	NCBI36
NG_009557.1:g.39451G= , LRG_27:g.39451G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2081G=
ENST00000695652.1:c.3610G=	ENSP00000512083.1:p.Asp1204=
ENST00000695653.1:c.1642G=	ENSP00000512084.1:p.Asp548=
ENST00000695654.1:c.2758G=	ENSP00000512085.1:p.Asp920=
ENST00000695655.1:c.2674G=	ENSP00000512086.1:n.2674G=
ENST00000695692.1:n.3097G=
ENST00000245907.11:c.3733G= MANE Select	ENSP00000245907.4:p.Asp1245=
ENST00000245907.10:c.3733G=	ENSP00000245907.4:p.Asp1245=
ENST00000596238.1:n.176G=
ENST00000601008.1:c.241+545G=	ENSP00000471384.1:n.241+545G=
NM_000064.3:c.3733G=	NP_000055.2:p.Asp1245=
NM_000064.4:c.3733G= MANE Select	NP_000055.2:p.Asp1245=