Canonical Allele Identifier: CA2320559221

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697784C= , CM000681.2:g.6697784C=	GRCh38
NC_000019.9:g.6697795C= , CM000681.1:g.6697795C=	GRCh37
NC_000019.8:g.6648795C=	NCBI36
NG_009557.1:g.27868G= , LRG_27:g.27868G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.799G=
ENST00000695652.1:c.2328G=	ENSP00000512083.1:p.Val776=
ENST00000695653.1:c.360G=	ENSP00000512084.1:p.Val120=
ENST00000695654.1:c.1575G=	ENSP00000512085.1:p.Val525=
ENST00000695655.1:c.1392G=	ENSP00000512086.1:n.1392G=
ENST00000695692.1:n.1815G=
ENST00000245907.11:c.2451G= MANE Select	ENSP00000245907.4:p.Val817=
ENST00000245907.10:c.2451G=	ENSP00000245907.4:p.Val817=
ENST00000602053.1:n.499G=
NM_000064.3:c.2451G=	NP_000055.2:p.Val817=
NM_000064.4:c.2451G= MANE Select	NP_000055.2:p.Val817=