Canonical Allele Identifier: CA2320559290

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697932C= , CM000681.2:g.6697932C=	GRCh38
NC_000019.9:g.6697943C= , CM000681.1:g.6697943C=	GRCh37
NC_000019.8:g.6648943C=	NCBI36
NG_009557.1:g.27720G= , LRG_27:g.27720G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-138G=
ENST00000695652.1:c.2318-138G=	ENSP00000512083.1:n.2318-138G=
ENST00000695653.1:c.350-138G=	ENSP00000512084.1:n.350-138G=
ENST00000695654.1:c.1565-138G=	ENSP00000512085.1:n.1565-138G=
ENST00000695655.1:c.1382-138G=	ENSP00000512086.1:n.1382-138G=
ENST00000695692.1:n.1805-138G=
ENST00000245907.11:c.2441-138G= MANE Select	ENSP00000245907.4:n.2441-138G=
ENST00000245907.10:c.2441-138G=	ENSP00000245907.4:n.2441-138G=
ENST00000602053.1:n.489-138G=
NM_000064.3:c.2441-138G=	NP_000055.2:n.2441-138G=
NM_000064.4:c.2441-138G= MANE Select	NP_000055.2:n.2441-138G=