Canonical Allele Identifier: CA2320567690

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712868T= , CM000681.2:g.6712868T=	GRCh38
NC_000019.9:g.6712879T= , CM000681.1:g.6712879T=	GRCh37
NC_000019.8:g.6663879T=	NCBI36
NG_009557.1:g.12784A= , LRG_27:g.12784A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.881-245A=	ENSP00000512083.1:n.881-245A=
ENST00000695654.1:c.128-245A=	ENSP00000512085.1:n.128-245A=
ENST00000695692.1:n.328-205A=
ENST00000245907.11:c.1004-245A= MANE Select	ENSP00000245907.4:n.1004-245A=
ENST00000245907.10:c.1004-245A=	ENSP00000245907.4:n.1004-245A=
ENST00000594270.5:n.128-266A=
ENST00000595577.1:n.508-245A=
ENST00000597442.5:n.254-245A=
NM_000064.3:c.1004-245A=	NP_000055.2:n.1004-245A=
NM_000064.4:c.1004-245A= MANE Select	NP_000055.2:n.1004-245A=