Canonical Allele Identifier: CA2320559041

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697367C= , CM000681.2:g.6697367C=	GRCh38
NC_000019.9:g.6697378C= , CM000681.1:g.6697378C=	GRCh37
NC_000019.8:g.6648378C=	NCBI36
NG_009557.1:g.28285G= , LRG_27:g.28285G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1121G=
ENST00000695652.1:c.2650G=	ENSP00000512083.1:p.Val884=
ENST00000695653.1:c.682G=	ENSP00000512084.1:p.Val228=
ENST00000695654.1:c.1897G=	ENSP00000512085.1:p.Val633=
ENST00000695655.1:c.1714G=	ENSP00000512086.1:n.1714G=
ENST00000695692.1:n.2137G=
ENST00000245907.11:c.2773G= MANE Select	ENSP00000245907.4:p.Val925=
ENST00000245907.10:c.2773G=	ENSP00000245907.4:p.Val925=
ENST00000594005.1:n.349G=
NM_000064.3:c.2773G=	NP_000055.2:p.Val925=
NM_000064.4:c.2773G= MANE Select	NP_000055.2:p.Val925=