Canonical Allele Identifier: CA2320567831

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713225A= , CM000681.2:g.6713225A=	GRCh38
NC_000019.9:g.6713236A= , CM000681.1:g.6713236A=	GRCh37
NC_000019.8:g.6664236A=	NCBI36
NG_009557.1:g.12427T= , LRG_27:g.12427T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.844T=	ENSP00000512083.1:p.Ser282=
ENST00000695654.1:c.91T=	ENSP00000512085.1:p.Ser31=
ENST00000695692.1:n.291T=
ENST00000245907.11:c.967T= MANE Select	ENSP00000245907.4:p.Ser323=
ENST00000245907.10:c.967T=	ENSP00000245907.4:p.Ser323=
ENST00000594270.5:n.91T=
ENST00000595577.1:n.471T=
ENST00000597442.5:n.217T=
NM_000064.3:c.967T=	NP_000055.2:p.Ser323=
NM_000064.4:c.967T= MANE Select	NP_000055.2:p.Ser323=