Canonical Allele Identifier: CA2320551543

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681974G= , CM000681.2:g.6681974G=	GRCh38
NC_000019.9:g.6681985G= , CM000681.1:g.6681985G=	GRCh37
NC_000019.8:g.6632985G=	NCBI36
NG_009557.1:g.43678C= , LRG_27:g.43678C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2665C=
ENST00000695653.1:c.2226C=	ENSP00000512084.1:p.Ser742=
ENST00000695654.1:c.3342C=	ENSP00000512085.1:p.Ser1114=
ENST00000695689.1:c.288C=	ENSP00000512101.1:n.288C=
ENST00000695690.1:n.508C=
ENST00000695691.1:n.508C=
ENST00000245907.11:c.4317C= MANE Select	ENSP00000245907.4:p.Ser1439=
ENST00000245907.10:c.4317C=	ENSP00000245907.4:p.Ser1439=
ENST00000596548.1:c.438C=	ENSP00000469744.1:p.Ser146=
ENST00000599899.5:n.1276C=
ENST00000601008.1:c.242-4016C=	ENSP00000471384.1:n.242-4016C=
NM_000064.3:c.4317C=	NP_000055.2:p.Ser1439=
NM_000064.4:c.4317C= MANE Select	NP_000055.2:p.Ser1439=