Canonical Allele Identifier: CA2320567689

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712860C= , CM000681.2:g.6712860C=	GRCh38
NC_000019.9:g.6712871C= , CM000681.1:g.6712871C=	GRCh37
NC_000019.8:g.6663871C=	NCBI36
NG_009557.1:g.12792G= , LRG_27:g.12792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.881-237G=	ENSP00000512083.1:n.881-237G=
ENST00000695654.1:c.128-237G=	ENSP00000512085.1:n.128-237G=
ENST00000695692.1:n.328-197G=
ENST00000245907.11:c.1004-237G= MANE Select	ENSP00000245907.4:n.1004-237G=
ENST00000245907.10:c.1004-237G=	ENSP00000245907.4:n.1004-237G=
ENST00000594270.5:n.128-258G=
ENST00000595577.1:n.508-237G=
ENST00000597442.5:n.254-237G=
NM_000064.3:c.1004-237G=	NP_000055.2:n.1004-237G=
NM_000064.4:c.1004-237G= MANE Select	NP_000055.2:n.1004-237G=