Canonical Allele Identifier: CA2320551652

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682226G= , CM000681.2:g.6682226G=	GRCh38
NC_000019.9:g.6682237G= , CM000681.1:g.6682237G=	GRCh37
NC_000019.8:g.6633237G=	NCBI36
NG_009557.1:g.43426C= , LRG_27:g.43426C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2524C=
ENST00000695653.1:c.2085C=	ENSP00000512084.1:p.Tyr695=
ENST00000695654.1:c.3201C=	ENSP00000512085.1:p.Tyr1067=
ENST00000695689.1:c.147C=	ENSP00000512101.1:n.147C=
ENST00000695690.1:n.367C=
ENST00000695691.1:n.367C=
ENST00000245907.11:c.4176C= MANE Select	ENSP00000245907.4:p.Tyr1392=
ENST00000245907.10:c.4176C=	ENSP00000245907.4:p.Tyr1392=
ENST00000596548.1:c.297C=	ENSP00000469744.1:p.Tyr99=
ENST00000599899.5:n.1135C=
ENST00000601008.1:c.242-4268C=	ENSP00000471384.1:n.242-4268C=
NM_000064.3:c.4176C=	NP_000055.2:p.Tyr1392=
NM_000064.4:c.4176C= MANE Select	NP_000055.2:p.Tyr1392=