Canonical Allele Identifier: CA2320551640

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682198T= , CM000681.2:g.6682198T=	GRCh38
NC_000019.9:g.6682209T= , CM000681.1:g.6682209T=	GRCh37
NC_000019.8:g.6633209T=	NCBI36
NG_009557.1:g.43454A= , LRG_27:g.43454A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2552A=
ENST00000695653.1:c.2113A=	ENSP00000512084.1:p.Ile705=
ENST00000695654.1:c.3229A=	ENSP00000512085.1:p.Ile1077=
ENST00000695689.1:c.175A=	ENSP00000512101.1:n.175A=
ENST00000695690.1:n.395A=
ENST00000695691.1:n.395A=
ENST00000245907.11:c.4204A= MANE Select	ENSP00000245907.4:p.Ile1402=
ENST00000245907.10:c.4204A=	ENSP00000245907.4:p.Ile1402=
ENST00000596548.1:c.325A=	ENSP00000469744.1:p.Ile109=
ENST00000599899.5:n.1163A=
ENST00000601008.1:c.242-4240A=	ENSP00000471384.1:n.242-4240A=
NM_000064.3:c.4204A=	NP_000055.2:p.Ile1402=
NM_000064.4:c.4204A= MANE Select	NP_000055.2:p.Ile1402=