Canonical Allele Identifier: CA2320550462

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679529T= , CM000681.2:g.6679529T=	GRCh38
NC_000019.9:g.6679540T= , CM000681.1:g.6679540T=	GRCh37
NC_000019.8:g.6630540T=	NCBI36
NG_009557.1:g.46123A= , LRG_27:g.46123A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805-33A=
ENST00000695653.1:c.2366-33A=	ENSP00000512084.1:n.2366-33A=
ENST00000695654.1:c.3482-33A=	ENSP00000512085.1:n.3482-33A=
ENST00000695689.1:c.428-33A=	ENSP00000512101.1:n.428-33A=
ENST00000695690.1:n.1522-33A=
ENST00000695691.1:n.1318-33A=
ENST00000245907.11:c.4457-33A= MANE Select	ENSP00000245907.4:n.4457-33A=
ENST00000245907.10:c.4457-33A=	ENSP00000245907.4:n.4457-33A=
ENST00000599668.1:n.52-33A=
ENST00000599899.5:n.1416-33A=
ENST00000601008.1:c.242-1571A=	ENSP00000471384.1:n.242-1571A=
NM_000064.3:c.4457-33A=	NP_000055.2:n.4457-33A=
NM_000064.4:c.4457-33A= MANE Select	NP_000055.2:n.4457-33A=