Canonical Allele Identifier: CA2320552850

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684969C= , CM000681.2:g.6684969C=	GRCh38
NC_000019.9:g.6684980C= , CM000681.1:g.6684980C=	GRCh37
NC_000019.8:g.6635980C=	NCBI36
NG_009557.1:g.40683G= , LRG_27:g.40683G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2317+19G=
ENST00000695653.1:c.1878+19G=	ENSP00000512084.1:n.1878+19G=
ENST00000695654.1:c.2994+19G=	ENSP00000512085.1:n.2994+19G=
ENST00000695690.1:n.160+19G=
ENST00000695691.1:n.160+19G=
ENST00000245907.11:c.3969+19G= MANE Select	ENSP00000245907.4:n.3969+19G=
ENST00000245907.10:c.3969+19G=	ENSP00000245907.4:n.3969+19G=
ENST00000596238.1:n.412+19G=
ENST00000596548.1:c.51+19G=	ENSP00000469744.1:n.51+19G=
ENST00000601008.1:c.241+1777G=	ENSP00000471384.1:n.241+1777G=
NM_000064.3:c.3969+19G=	NP_000055.2:n.3969+19G=
NM_000064.4:c.3969+19G= MANE Select	NP_000055.2:n.3969+19G=