Canonical Allele Identifier: CA2320559152

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697616C= , CM000681.2:g.6697616C=	GRCh38
NC_000019.9:g.6697627C= , CM000681.1:g.6697627C=	GRCh37
NC_000019.8:g.6648627C=	NCBI36
NG_009557.1:g.28036G= , LRG_27:g.28036G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.931+36G=
ENST00000695652.1:c.2460+36G=	ENSP00000512083.1:n.2460+36G=
ENST00000695653.1:c.492+36G=	ENSP00000512084.1:n.492+36G=
ENST00000695654.1:c.1707+36G=	ENSP00000512085.1:n.1707+36G=
ENST00000695655.1:c.1524+36G=	ENSP00000512086.1:n.1524+36G=
ENST00000695692.1:n.1947+36G=
ENST00000245907.11:c.2583+36G= MANE Select	ENSP00000245907.4:n.2583+36G=
ENST00000245907.10:c.2583+36G=	ENSP00000245907.4:n.2583+36G=
ENST00000594005.1:n.100G=
NM_000064.3:c.2583+36G=	NP_000055.2:n.2583+36G=
NM_000064.4:c.2583+36G= MANE Select	NP_000055.2:n.2583+36G=