Canonical Allele Identifier: CA2320552860

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684997T= , CM000681.2:g.6684997T=	GRCh38
NC_000019.9:g.6685008T= , CM000681.1:g.6685008T=	GRCh37
NC_000019.8:g.6636008T=	NCBI36
NG_009557.1:g.40655A= , LRG_27:g.40655A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2308A=
ENST00000695653.1:c.1869A=	ENSP00000512084.1:p.Arg623=
ENST00000695654.1:c.2985A=	ENSP00000512085.1:p.Arg995=
ENST00000695690.1:n.151A=
ENST00000695691.1:n.151A=
ENST00000245907.11:c.3960A= MANE Select	ENSP00000245907.4:p.Arg1320=
ENST00000245907.10:c.3960A=	ENSP00000245907.4:p.Arg1320=
ENST00000596238.1:n.403A=
ENST00000596548.1:c.42A=	ENSP00000469744.1:p.Arg14=
ENST00000601008.1:c.241+1749A=	ENSP00000471384.1:n.241+1749A=
NM_000064.3:c.3960A=	NP_000055.2:p.Arg1320=
NM_000064.4:c.3960A= MANE Select	NP_000055.2:p.Arg1320=