Canonical Allele Identifier: CA2320552871

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685034G= , CM000681.2:g.6685034G=	GRCh38
NC_000019.9:g.6685045G= , CM000681.1:g.6685045G=	GRCh37
NC_000019.8:g.6636045G=	NCBI36
NG_009557.1:g.40618C= , LRG_27:g.40618C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2271C=
ENST00000695653.1:c.1832C=	ENSP00000512084.1:p.Thr611=
ENST00000695654.1:c.2948C=	ENSP00000512085.1:p.Thr983=
ENST00000695690.1:n.114C=
ENST00000695691.1:n.114C=
ENST00000245907.11:c.3923C= MANE Select	ENSP00000245907.4:p.Thr1308=
ENST00000245907.10:c.3923C=	ENSP00000245907.4:p.Thr1308=
ENST00000596238.1:n.366C=
ENST00000596548.1:c.5C=	ENSP00000469744.1:p.Thr2=
ENST00000601008.1:c.241+1712C=	ENSP00000471384.1:n.241+1712C=
NM_000064.3:c.3923C=	NP_000055.2:p.Thr1308=
NM_000064.4:c.3923C= MANE Select	NP_000055.2:p.Thr1308=