Canonical Allele Identifier: CA2320552867

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685019C= , CM000681.2:g.6685019C=	GRCh38
NC_000019.9:g.6685030C= , CM000681.1:g.6685030C=	GRCh37
NC_000019.8:g.6636030C=	NCBI36
NG_009557.1:g.40633G= , LRG_27:g.40633G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2286G=
ENST00000695653.1:c.1847G=	ENSP00000512084.1:p.Trp616=
ENST00000695654.1:c.2963G=	ENSP00000512085.1:p.Trp988=
ENST00000695690.1:n.129G=
ENST00000695691.1:n.129G=
ENST00000245907.11:c.3938G= MANE Select	ENSP00000245907.4:p.Trp1313=
ENST00000245907.10:c.3938G=	ENSP00000245907.4:p.Trp1313=
ENST00000596238.1:n.381G=
ENST00000596548.1:c.20G=	ENSP00000469744.1:p.Trp7=
ENST00000601008.1:c.241+1727G=	ENSP00000471384.1:n.241+1727G=
NM_000064.3:c.3938G=	NP_000055.2:p.Trp1313=
NM_000064.4:c.3938G= MANE Select	NP_000055.2:p.Trp1313=