Canonical Allele Identifier: CA2320559070

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697461C= , CM000681.2:g.6697461C=	GRCh38
NC_000019.9:g.6697472C= , CM000681.1:g.6697472C=	GRCh37
NC_000019.8:g.6648472C=	NCBI36
NG_009557.1:g.28191G= , LRG_27:g.28191G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1027G=
ENST00000695652.1:c.2556G=	ENSP00000512083.1:p.Ser852=
ENST00000695653.1:c.588G=	ENSP00000512084.1:p.Ser196=
ENST00000695654.1:c.1803G=	ENSP00000512085.1:p.Ser601=
ENST00000695655.1:c.1620G=	ENSP00000512086.1:n.1620G=
ENST00000695692.1:n.2043G=
ENST00000245907.11:c.2679G= MANE Select	ENSP00000245907.4:p.Ser893=
ENST00000245907.10:c.2679G=	ENSP00000245907.4:p.Ser893=
ENST00000594005.1:n.255G=
NM_000064.3:c.2679G=	NP_000055.2:p.Ser893=
NM_000064.4:c.2679G= MANE Select	NP_000055.2:p.Ser893=