Canonical Allele Identifier: CA2320559059

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697435G= , CM000681.2:g.6697435G=	GRCh38
NC_000019.9:g.6697446G= , CM000681.1:g.6697446G=	GRCh37
NC_000019.8:g.6648446G=	NCBI36
NG_009557.1:g.28217C= , LRG_27:g.28217C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1053C=
ENST00000695652.1:c.2582C=	ENSP00000512083.1:p.Pro861=
ENST00000695653.1:c.614C=	ENSP00000512084.1:p.Pro205=
ENST00000695654.1:c.1829C=	ENSP00000512085.1:p.Pro610=
ENST00000695655.1:c.1646C=	ENSP00000512086.1:n.1646C=
ENST00000695692.1:n.2069C=
ENST00000245907.11:c.2705C= MANE Select	ENSP00000245907.4:p.Pro902=
ENST00000245907.10:c.2705C=	ENSP00000245907.4:p.Pro902=
ENST00000594005.1:n.281C=
NM_000064.3:c.2705C=	NP_000055.2:p.Pro902=
NM_000064.4:c.2705C= MANE Select	NP_000055.2:p.Pro902=