Canonical Allele Identifier: CA2320551552

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681995A= , CM000681.2:g.6681995A=	GRCh38
NC_000019.9:g.6682006A= , CM000681.1:g.6682006A=	GRCh37
NC_000019.8:g.6633006A=	NCBI36
NG_009557.1:g.43657T= , LRG_27:g.43657T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2644T=
ENST00000695653.1:c.2205T=	ENSP00000512084.1:p.Tyr735=
ENST00000695654.1:c.3321T=	ENSP00000512085.1:p.Tyr1107=
ENST00000695689.1:c.267T=	ENSP00000512101.1:n.267T=
ENST00000695690.1:n.487T=
ENST00000695691.1:n.487T=
ENST00000245907.11:c.4296T= MANE Select	ENSP00000245907.4:p.Tyr1432=
ENST00000245907.10:c.4296T=	ENSP00000245907.4:p.Tyr1432=
ENST00000596548.1:c.417T=	ENSP00000469744.1:p.Tyr139=
ENST00000599899.5:n.1255T=
ENST00000601008.1:c.242-4037T=	ENSP00000471384.1:n.242-4037T=
NM_000064.3:c.4296T=	NP_000055.2:p.Tyr1432=
NM_000064.4:c.4296T= MANE Select	NP_000055.2:p.Tyr1432=