Canonical Allele Identifier: CA2320559192

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697714G= , CM000681.2:g.6697714G=	GRCh38
NC_000019.9:g.6697725G= , CM000681.1:g.6697725G=	GRCh37
NC_000019.8:g.6648725G=	NCBI36
NG_009557.1:g.27938C= , LRG_27:g.27938C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.869C=
ENST00000695652.1:c.2398C=	ENSP00000512083.1:p.Arg800=
ENST00000695653.1:c.430C=	ENSP00000512084.1:p.Arg144=
ENST00000695654.1:c.1645C=	ENSP00000512085.1:p.Arg549=
ENST00000695655.1:c.1462C=	ENSP00000512086.1:n.1462C=
ENST00000695692.1:n.1885C=
ENST00000245907.11:c.2521C= MANE Select	ENSP00000245907.4:p.Arg841=
ENST00000245907.10:c.2521C=	ENSP00000245907.4:p.Arg841=
ENST00000594005.1:n.2C=
ENST00000602053.1:n.569C=
NM_000064.3:c.2521C=	NP_000055.2:p.Arg841=
NM_000064.4:c.2521C= MANE Select	NP_000055.2:p.Arg841=