Canonical Allele Identifier: CA2320559099

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697511T= , CM000681.2:g.6697511T=	GRCh38
NC_000019.9:g.6697522T= , CM000681.1:g.6697522T=	GRCh37
NC_000019.8:g.6648522T=	NCBI36
NG_009557.1:g.28141A= , LRG_27:g.28141A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.977A=
ENST00000695652.1:c.2506A=	ENSP00000512083.1:p.Thr836=
ENST00000695653.1:c.538A=	ENSP00000512084.1:p.Thr180=
ENST00000695654.1:c.1753A=	ENSP00000512085.1:p.Thr585=
ENST00000695655.1:c.1570A=	ENSP00000512086.1:n.1570A=
ENST00000695692.1:n.1993A=
ENST00000245907.11:c.2629A= MANE Select	ENSP00000245907.4:p.Thr877=
ENST00000245907.10:c.2629A=	ENSP00000245907.4:p.Thr877=
ENST00000594005.1:n.205A=
NM_000064.3:c.2629A=	NP_000055.2:p.Thr877=
NM_000064.4:c.2629A= MANE Select	NP_000055.2:p.Thr877=