Canonical Allele Identifier: CA2320551563

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682028C= , CM000681.2:g.6682028C=	GRCh38
NC_000019.9:g.6682039C= , CM000681.1:g.6682039C=	GRCh37
NC_000019.8:g.6633039C=	NCBI36
NG_009557.1:g.43624G= , LRG_27:g.43624G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2611G=
ENST00000695653.1:c.2172G=	ENSP00000512084.1:p.Leu724=
ENST00000695654.1:c.3288G=	ENSP00000512085.1:p.Leu1096=
ENST00000695689.1:c.234G=	ENSP00000512101.1:n.234G=
ENST00000695690.1:n.454G=
ENST00000695691.1:n.454G=
ENST00000245907.11:c.4263G= MANE Select	ENSP00000245907.4:p.Leu1421=
ENST00000245907.10:c.4263G=	ENSP00000245907.4:p.Leu1421=
ENST00000596548.1:c.384G=	ENSP00000469744.1:p.Leu128=
ENST00000599899.5:n.1222G=
ENST00000601008.1:c.242-4070G=	ENSP00000471384.1:n.242-4070G=
NM_000064.3:c.4263G=	NP_000055.2:p.Leu1421=
NM_000064.4:c.4263G= MANE Select	NP_000055.2:p.Leu1421=