Canonical Allele Identifier: CA2320559052

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697419C= , CM000681.2:g.6697419C=	GRCh38
NC_000019.9:g.6697430C= , CM000681.1:g.6697430C=	GRCh37
NC_000019.8:g.6648430C=	NCBI36
NG_009557.1:g.28233G= , LRG_27:g.28233G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1069G=
ENST00000695652.1:c.2598G=	ENSP00000512083.1:p.Leu866=
ENST00000695653.1:c.630G=	ENSP00000512084.1:p.Leu210=
ENST00000695654.1:c.1845G=	ENSP00000512085.1:p.Leu615=
ENST00000695655.1:c.1662G=	ENSP00000512086.1:n.1662G=
ENST00000695692.1:n.2085G=
ENST00000245907.11:c.2721G= MANE Select	ENSP00000245907.4:p.Leu907=
ENST00000245907.10:c.2721G=	ENSP00000245907.4:p.Leu907=
ENST00000594005.1:n.297G=
NM_000064.3:c.2721G=	NP_000055.2:p.Leu907=
NM_000064.4:c.2721G= MANE Select	NP_000055.2:p.Leu907=