Canonical Allele Identifier: CA2320551654

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682228A= , CM000681.2:g.6682228A=	GRCh38
NC_000019.9:g.6682239A= , CM000681.1:g.6682239A=	GRCh37
NC_000019.8:g.6633239A=	NCBI36
NG_009557.1:g.43424T= , LRG_27:g.43424T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2522T=
ENST00000695653.1:c.2083T=	ENSP00000512084.1:p.Tyr695=
ENST00000695654.1:c.3199T=	ENSP00000512085.1:p.Tyr1067=
ENST00000695689.1:c.145T=	ENSP00000512101.1:n.145T=
ENST00000695690.1:n.365T=
ENST00000695691.1:n.365T=
ENST00000245907.11:c.4174T= MANE Select	ENSP00000245907.4:p.Tyr1392=
ENST00000245907.10:c.4174T=	ENSP00000245907.4:p.Tyr1392=
ENST00000596548.1:c.295T=	ENSP00000469744.1:p.Tyr99=
ENST00000599899.5:n.1133T=
ENST00000601008.1:c.242-4270T=	ENSP00000471384.1:n.242-4270T=
NM_000064.3:c.4174T=	NP_000055.2:p.Tyr1392=
NM_000064.4:c.4174T= MANE Select	NP_000055.2:p.Tyr1392=