Canonical Allele Identifier: CA2320559048

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697402T= , CM000681.2:g.6697402T=	GRCh38
NC_000019.9:g.6697413T= , CM000681.1:g.6697413T=	GRCh37
NC_000019.8:g.6648413T=	NCBI36
NG_009557.1:g.28250A= , LRG_27:g.28250A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1086A=
ENST00000695652.1:c.2615A=	ENSP00000512083.1:p.Lys872=
ENST00000695653.1:c.647A=	ENSP00000512084.1:p.Lys216=
ENST00000695654.1:c.1862A=	ENSP00000512085.1:p.Lys621=
ENST00000695655.1:c.1679A=	ENSP00000512086.1:n.1679A=
ENST00000695692.1:n.2102A=
ENST00000245907.11:c.2738A= MANE Select	ENSP00000245907.4:p.Lys913=
ENST00000245907.10:c.2738A=	ENSP00000245907.4:p.Lys913=
ENST00000594005.1:n.314A=
NM_000064.3:c.2738A=	NP_000055.2:p.Lys913=
NM_000064.4:c.2738A= MANE Select	NP_000055.2:p.Lys913=