Canonical Allele Identifier: CA2320559037

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697356G= , CM000681.2:g.6697356G=	GRCh38
NC_000019.9:g.6697367G= , CM000681.1:g.6697367G=	GRCh37
NC_000019.8:g.6648367G=	NCBI36
NG_009557.1:g.28296C= , LRG_27:g.28296C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1132C=
ENST00000695652.1:c.2661C=	ENSP00000512083.1:p.Ser887=
ENST00000695653.1:c.693C=	ENSP00000512084.1:p.Ser231=
ENST00000695654.1:c.1908C=	ENSP00000512085.1:p.Ser636=
ENST00000695655.1:c.1725C=	ENSP00000512086.1:n.1725C=
ENST00000695692.1:n.2148C=
ENST00000245907.11:c.2784C= MANE Select	ENSP00000245907.4:p.Ser928=
ENST00000245907.10:c.2784C=	ENSP00000245907.4:p.Ser928=
ENST00000594005.1:n.360C=
NM_000064.3:c.2784C=	NP_000055.2:p.Ser928=
NM_000064.4:c.2784C= MANE Select	NP_000055.2:p.Ser928=