Canonical Allele Identifier: CA2320552905

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685108T= , CM000681.2:g.6685108T=	GRCh38
NC_000019.9:g.6685119T= , CM000681.1:g.6685119T=	GRCh37
NC_000019.8:g.6636119T=	NCBI36
NG_009557.1:g.40544A= , LRG_27:g.40544A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2197A=
ENST00000695653.1:c.1758A=	ENSP00000512084.1:p.Gln586=
ENST00000695654.1:c.2874A=	ENSP00000512085.1:p.Gln958=
ENST00000695690.1:n.40A=
ENST00000695691.1:n.40A=
ENST00000245907.11:c.3849A= MANE Select	ENSP00000245907.4:p.Gln1283=
ENST00000245907.10:c.3849A=	ENSP00000245907.4:p.Gln1283=
ENST00000596238.1:n.292A=
ENST00000601008.1:c.241+1638A=	ENSP00000471384.1:n.241+1638A=
NM_000064.3:c.3849A=	NP_000055.2:p.Gln1283=
NM_000064.4:c.3849A= MANE Select	NP_000055.2:p.Gln1283=