Canonical Allele Identifier: CA2320550280

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679168C= , CM000681.2:g.6679168C=	GRCh38
NC_000019.9:g.6679179C= , CM000681.1:g.6679179C=	GRCh37
NC_000019.8:g.6630179C=	NCBI36
NG_009557.1:g.46484G= , LRG_27:g.46484G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2935G=
ENST00000695653.1:c.2496G=	ENSP00000512084.1:p.Leu832=
ENST00000695654.1:c.3612G=	ENSP00000512085.1:p.Leu1204=
ENST00000695689.1:c.558G=	ENSP00000512101.1:n.558G=
ENST00000695690.1:n.1652G=
ENST00000695691.1:n.1448G=
ENST00000245907.11:c.4587G= MANE Select	ENSP00000245907.4:p.Leu1529=
ENST00000245907.10:c.4587G=	ENSP00000245907.4:p.Leu1529=
ENST00000599668.1:n.207G=
ENST00000599899.5:n.1546G=
ENST00000601008.1:c.242-1210G=	ENSP00000471384.1:n.242-1210G=
ENST00000602229.1:c.34G=
NM_000064.3:c.4587G=	NP_000055.2:p.Leu1529=
NM_000064.4:c.4587G= MANE Select	NP_000055.2:p.Leu1529=