Canonical Allele Identifier: CA2320559058

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697434C= , CM000681.2:g.6697434C=	GRCh38
NC_000019.9:g.6697445C= , CM000681.1:g.6697445C=	GRCh37
NC_000019.8:g.6648445C=	NCBI36
NG_009557.1:g.28218G= , LRG_27:g.28218G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1054G=
ENST00000695652.1:c.2583G=	ENSP00000512083.1:p.Pro861=
ENST00000695653.1:c.615G=	ENSP00000512084.1:p.Pro205=
ENST00000695654.1:c.1830G=	ENSP00000512085.1:p.Pro610=
ENST00000695655.1:c.1647G=	ENSP00000512086.1:n.1647G=
ENST00000695692.1:n.2070G=
ENST00000245907.11:c.2706G= MANE Select	ENSP00000245907.4:p.Pro902=
ENST00000245907.10:c.2706G=	ENSP00000245907.4:p.Pro902=
ENST00000594005.1:n.282G=
NM_000064.3:c.2706G=	NP_000055.2:p.Pro902=
NM_000064.4:c.2706G= MANE Select	NP_000055.2:p.Pro902=