Canonical Allele Identifier: CA2320551544

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681975G= , CM000681.2:g.6681975G=	GRCh38
NC_000019.9:g.6681986G= , CM000681.1:g.6681986G=	GRCh37
NC_000019.8:g.6632986G=	NCBI36
NG_009557.1:g.43677C= , LRG_27:g.43677C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2664C=
ENST00000695653.1:c.2225C=	ENSP00000512084.1:p.Ser742=
ENST00000695654.1:c.3341C=	ENSP00000512085.1:p.Ser1114=
ENST00000695689.1:c.287C=	ENSP00000512101.1:n.287C=
ENST00000695690.1:n.507C=
ENST00000695691.1:n.507C=
ENST00000245907.11:c.4316C= MANE Select	ENSP00000245907.4:p.Ser1439=
ENST00000245907.10:c.4316C=	ENSP00000245907.4:p.Ser1439=
ENST00000596548.1:c.437C=	ENSP00000469744.1:p.Ser146=
ENST00000599899.5:n.1275C=
ENST00000601008.1:c.242-4017C=	ENSP00000471384.1:n.242-4017C=
NM_000064.3:c.4316C=	NP_000055.2:p.Ser1439=
NM_000064.4:c.4316C= MANE Select	NP_000055.2:p.Ser1439=