Canonical Allele Identifier: CA2320559034

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697349C= , CM000681.2:g.6697349C=	GRCh38
NC_000019.9:g.6697360C= , CM000681.1:g.6697360C=	GRCh37
NC_000019.8:g.6648360C=	NCBI36
NG_009557.1:g.28303G= , LRG_27:g.28303G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1139G=
ENST00000695652.1:c.2668G=	ENSP00000512083.1:p.Val890=
ENST00000695653.1:c.700G=	ENSP00000512084.1:p.Val234=
ENST00000695654.1:c.1915G=	ENSP00000512085.1:p.Val639=
ENST00000695655.1:c.1732G=	ENSP00000512086.1:n.1732G=
ENST00000695692.1:n.2155G=
ENST00000245907.11:c.2791G= MANE Select	ENSP00000245907.4:p.Val931=
ENST00000245907.10:c.2791G=	ENSP00000245907.4:p.Val931=
ENST00000594005.1:n.367G=
NM_000064.3:c.2791G=	NP_000055.2:p.Val931=
NM_000064.4:c.2791G= MANE Select	NP_000055.2:p.Val931=