Canonical Allele Identifier: CA2320550433

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679470G= , CM000681.2:g.6679470G=	GRCh38
NC_000019.9:g.6679481G= , CM000681.1:g.6679481G=	GRCh37
NC_000019.8:g.6630481G=	NCBI36
NG_009557.1:g.46182C= , LRG_27:g.46182C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2831C=
ENST00000695653.1:c.2392C=	ENSP00000512084.1:p.Pro798=
ENST00000695654.1:c.3508C=	ENSP00000512085.1:p.Pro1170=
ENST00000695689.1:c.454C=	ENSP00000512101.1:n.454C=
ENST00000695690.1:n.1548C=
ENST00000695691.1:n.1344C=
ENST00000245907.11:c.4483C= MANE Select	ENSP00000245907.4:p.Pro1495=
ENST00000245907.10:c.4483C=	ENSP00000245907.4:p.Pro1495=
ENST00000599668.1:n.78C=
ENST00000599899.5:n.1442C=
ENST00000601008.1:c.242-1512C=	ENSP00000471384.1:n.242-1512C=
NM_000064.3:c.4483C=	NP_000055.2:p.Pro1495=
NM_000064.4:c.4483C= MANE Select	NP_000055.2:p.Pro1495=