Canonical Allele Identifier: CA2320557795

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6694917T= , CM000681.2:g.6694917T=	GRCh38
NC_000019.9:g.6694928T= , CM000681.1:g.6694928T=	GRCh37
NC_000019.8:g.6645928T=	NCBI36
NG_009557.1:g.30735A= , LRG_27:g.30735A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1299-283A=
ENST00000695652.1:c.2828-283A=	ENSP00000512083.1:n.2828-283A=
ENST00000695653.1:c.860-283A=	ENSP00000512084.1:n.860-283A=
ENST00000695654.1:c.2075-283A=	ENSP00000512085.1:n.2075-283A=
ENST00000695655.1:c.1892-283A=	ENSP00000512086.1:n.1892-283A=
ENST00000695692.1:n.2315-283A=
ENST00000245907.11:c.2951-283A= MANE Select	ENSP00000245907.4:n.2951-283A=
ENST00000245907.10:c.2951-283A=	ENSP00000245907.4:n.2951-283A=
NM_000064.3:c.2951-283A=	NP_000055.2:n.2951-283A=
NM_000064.4:c.2951-283A= MANE Select	NP_000055.2:n.2951-283A=