Canonical Allele Identifier: CA2320559074

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697468T= , CM000681.2:g.6697468T=	GRCh38
NC_000019.9:g.6697479T= , CM000681.1:g.6697479T=	GRCh37
NC_000019.8:g.6648479T=	NCBI36
NG_009557.1:g.28184A= , LRG_27:g.28184A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1020A=
ENST00000695652.1:c.2549A=	ENSP00000512083.1:p.Lys850=
ENST00000695653.1:c.581A=	ENSP00000512084.1:p.Lys194=
ENST00000695654.1:c.1796A=	ENSP00000512085.1:p.Lys599=
ENST00000695655.1:c.1613A=	ENSP00000512086.1:n.1613A=
ENST00000695692.1:n.2036A=
ENST00000245907.11:c.2672A= MANE Select	ENSP00000245907.4:p.Lys891=
ENST00000245907.10:c.2672A=	ENSP00000245907.4:p.Lys891=
ENST00000594005.1:n.248A=
NM_000064.3:c.2672A=	NP_000055.2:p.Lys891=
NM_000064.4:c.2672A= MANE Select	NP_000055.2:p.Lys891=