Canonical Allele Identifier: CA2320559388

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6698032A= , CM000681.2:g.6698032A=	GRCh38
NC_000019.9:g.6698043A= , CM000681.1:g.6698043A=	GRCh37
NC_000019.8:g.6649043A=	NCBI36
NG_009557.1:g.27620T= , LRG_27:g.27620T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-238T=
ENST00000695652.1:c.2318-238T=	ENSP00000512083.1:n.2318-238T=
ENST00000695653.1:c.350-238T=	ENSP00000512084.1:n.350-238T=
ENST00000695654.1:c.1565-238T=	ENSP00000512085.1:n.1565-238T=
ENST00000695655.1:c.1382-238T=	ENSP00000512086.1:n.1382-238T=
ENST00000695692.1:n.1805-238T=
ENST00000245907.11:c.2441-238T= MANE Select	ENSP00000245907.4:n.2441-238T=
ENST00000245907.10:c.2441-238T=	ENSP00000245907.4:n.2441-238T=
ENST00000602053.1:n.489-238T=
NM_000064.3:c.2441-238T=	NP_000055.2:n.2441-238T=
NM_000064.4:c.2441-238T= MANE Select	NP_000055.2:n.2441-238T=