Canonical Allele Identifier: CA2320550427

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679456A= , CM000681.2:g.6679456A=	GRCh38
NC_000019.9:g.6679467A= , CM000681.1:g.6679467A=	GRCh37
NC_000019.8:g.6630467A=	NCBI36
NG_009557.1:g.46196T= , LRG_27:g.46196T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2845T=
ENST00000695653.1:c.2406T=	ENSP00000512084.1:p.Asp802=
ENST00000695654.1:c.3522T=	ENSP00000512085.1:p.Asp1174=
ENST00000695689.1:c.468T=	ENSP00000512101.1:n.468T=
ENST00000695690.1:n.1562T=
ENST00000695691.1:n.1358T=
ENST00000245907.11:c.4497T= MANE Select	ENSP00000245907.4:p.Asp1499=
ENST00000245907.10:c.4497T=	ENSP00000245907.4:p.Asp1499=
ENST00000599668.1:n.92T=
ENST00000599899.5:n.1456T=
ENST00000601008.1:c.242-1498T=	ENSP00000471384.1:n.242-1498T=
NM_000064.3:c.4497T=	NP_000055.2:p.Asp1499=
NM_000064.4:c.4497T= MANE Select	NP_000055.2:p.Asp1499=