Canonical Allele Identifier: CA2320559061

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697440G= , CM000681.2:g.6697440G=	GRCh38
NC_000019.9:g.6697451G= , CM000681.1:g.6697451G=	GRCh37
NC_000019.8:g.6648451G=	NCBI36
NG_009557.1:g.28212C= , LRG_27:g.28212C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1048C=
ENST00000695652.1:c.2577C=	ENSP00000512083.1:p.Ile859=
ENST00000695653.1:c.609C=	ENSP00000512084.1:p.Ile203=
ENST00000695654.1:c.1824C=	ENSP00000512085.1:p.Ile608=
ENST00000695655.1:c.1641C=	ENSP00000512086.1:n.1641C=
ENST00000695692.1:n.2064C=
ENST00000245907.11:c.2700C= MANE Select	ENSP00000245907.4:p.Ile900=
ENST00000245907.10:c.2700C=	ENSP00000245907.4:p.Ile900=
ENST00000594005.1:n.276C=
NM_000064.3:c.2700C=	NP_000055.2:p.Ile900=
NM_000064.4:c.2700C= MANE Select	NP_000055.2:p.Ile900=