Canonical Allele Identifier: CA2320559086

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697485G= , CM000681.2:g.6697485G=	GRCh38
NC_000019.9:g.6697496G= , CM000681.1:g.6697496G=	GRCh37
NC_000019.8:g.6648496G=	NCBI36
NG_009557.1:g.28167C= , LRG_27:g.28167C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1003C=
ENST00000695652.1:c.2532C=	ENSP00000512083.1:p.Thr844=
ENST00000695653.1:c.564C=	ENSP00000512084.1:p.Thr188=
ENST00000695654.1:c.1779C=	ENSP00000512085.1:p.Thr593=
ENST00000695655.1:c.1596C=	ENSP00000512086.1:n.1596C=
ENST00000695692.1:n.2019C=
ENST00000245907.11:c.2655C= MANE Select	ENSP00000245907.4:p.Thr885=
ENST00000245907.10:c.2655C=	ENSP00000245907.4:p.Thr885=
ENST00000594005.1:n.231C=
NM_000064.3:c.2655C=	NP_000055.2:p.Thr885=
NM_000064.4:c.2655C= MANE Select	NP_000055.2:p.Thr885=