Canonical Allele Identifier: CA2320559065

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697449T= , CM000681.2:g.6697449T=	GRCh38
NC_000019.9:g.6697460T= , CM000681.1:g.6697460T=	GRCh37
NC_000019.8:g.6648460T=	NCBI36
NG_009557.1:g.28203A= , LRG_27:g.28203A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1039A=
ENST00000695652.1:c.2568A=	ENSP00000512083.1:p.Pro856=
ENST00000695653.1:c.600A=	ENSP00000512084.1:p.Pro200=
ENST00000695654.1:c.1815A=	ENSP00000512085.1:p.Pro605=
ENST00000695655.1:c.1632A=	ENSP00000512086.1:n.1632A=
ENST00000695692.1:n.2055A=
ENST00000245907.11:c.2691A= MANE Select	ENSP00000245907.4:p.Pro897=
ENST00000245907.10:c.2691A=	ENSP00000245907.4:p.Pro897=
ENST00000594005.1:n.267A=
NM_000064.3:c.2691A=	NP_000055.2:p.Pro897=
NM_000064.4:c.2691A= MANE Select	NP_000055.2:p.Pro897=