Canonical Allele Identifier: CA2320565912

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709694G= , CM000681.2:g.6709694G=	GRCh38
NC_000019.9:g.6709705G= , CM000681.1:g.6709705G=	GRCh37
NC_000019.8:g.6660705G=	NCBI36
NG_009557.1:g.15958C= , LRG_27:g.15958C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1712C=	ENSP00000512083.1:p.Thr571=
ENST00000695654.1:c.959C=	ENSP00000512085.1:p.Thr320=
ENST00000695655.1:c.776C=	ENSP00000512086.1:n.776C=
ENST00000695692.1:n.1199C=
ENST00000245907.11:c.1835C= MANE Select	ENSP00000245907.4:p.Thr612=
ENST00000245907.10:c.1835C=	ENSP00000245907.4:p.Thr612=
NM_000064.3:c.1835C=	NP_000055.2:p.Thr612=
NM_000064.4:c.1835C= MANE Select	NP_000055.2:p.Thr612=