Canonical Allele Identifier: CA2320553477

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686232G= , CM000681.2:g.6686232G=	GRCh38
NC_000019.9:g.6686243G= , CM000681.1:g.6686243G=	GRCh37
NC_000019.8:g.6637243G=	NCBI36
NG_009557.1:g.39420C= , LRG_27:g.39420C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2050C=
ENST00000695652.1:c.3579C=	ENSP00000512083.1:p.Ser1193=
ENST00000695653.1:c.1611C=	ENSP00000512084.1:p.Ser537=
ENST00000695654.1:c.2727C=	ENSP00000512085.1:p.Ser909=
ENST00000695655.1:c.2643C=	ENSP00000512086.1:n.2643C=
ENST00000695692.1:n.3066C=
ENST00000245907.11:c.3702C= MANE Select	ENSP00000245907.4:p.Ser1234=
ENST00000245907.10:c.3702C=	ENSP00000245907.4:p.Ser1234=
ENST00000596238.1:n.145C=
ENST00000601008.1:c.241+514C=	ENSP00000471384.1:n.241+514C=
NM_000064.3:c.3702C=	NP_000055.2:p.Ser1234=
NM_000064.4:c.3702C= MANE Select	NP_000055.2:p.Ser1234=