Canonical Allele Identifier: CA2320567678

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712843A= , CM000681.2:g.6712843A=	GRCh38
NC_000019.9:g.6712854A= , CM000681.1:g.6712854A=	GRCh37
NC_000019.8:g.6663854A=	NCBI36
NG_009557.1:g.12809T= , LRG_27:g.12809T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.881-220T=	ENSP00000512083.1:n.881-220T=
ENST00000695654.1:c.128-220T=	ENSP00000512085.1:n.128-220T=
ENST00000695692.1:n.328-180T=
ENST00000245907.11:c.1004-220T= MANE Select	ENSP00000245907.4:n.1004-220T=
ENST00000245907.10:c.1004-220T=	ENSP00000245907.4:n.1004-220T=
ENST00000594270.5:n.128-241T=
ENST00000595577.1:n.508-220T=
ENST00000597442.5:n.254-220T=
NM_000064.3:c.1004-220T=	NP_000055.2:n.1004-220T=
NM_000064.4:c.1004-220T= MANE Select	NP_000055.2:n.1004-220T=