Canonical Allele Identifier: CA2320559279

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697890C= , CM000681.2:g.6697890C=	GRCh38
NC_000019.9:g.6697901C= , CM000681.1:g.6697901C=	GRCh37
NC_000019.8:g.6648901C=	NCBI36
NG_009557.1:g.27762G= , LRG_27:g.27762G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-96G=
ENST00000695652.1:c.2318-96G=	ENSP00000512083.1:n.2318-96G=
ENST00000695653.1:c.350-96G=	ENSP00000512084.1:n.350-96G=
ENST00000695654.1:c.1565-96G=	ENSP00000512085.1:n.1565-96G=
ENST00000695655.1:c.1382-96G=	ENSP00000512086.1:n.1382-96G=
ENST00000695692.1:n.1805-96G=
ENST00000245907.11:c.2441-96G= MANE Select	ENSP00000245907.4:n.2441-96G=
ENST00000245907.10:c.2441-96G=	ENSP00000245907.4:n.2441-96G=
ENST00000602053.1:n.489-96G=
NM_000064.3:c.2441-96G=	NP_000055.2:n.2441-96G=
NM_000064.4:c.2441-96G= MANE Select	NP_000055.2:n.2441-96G=