Canonical Allele Identifier: CA2320559054

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697424C= , CM000681.2:g.6697424C=	GRCh38
NC_000019.9:g.6697435C= , CM000681.1:g.6697435C=	GRCh37
NC_000019.8:g.6648435C=	NCBI36
NG_009557.1:g.28228G= , LRG_27:g.28228G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1064G=
ENST00000695652.1:c.2593G=	ENSP00000512083.1:p.Gly865=
ENST00000695653.1:c.625G=	ENSP00000512084.1:p.Gly209=
ENST00000695654.1:c.1840G=	ENSP00000512085.1:p.Gly614=
ENST00000695655.1:c.1657G=	ENSP00000512086.1:n.1657G=
ENST00000695692.1:n.2080G=
ENST00000245907.11:c.2716G= MANE Select	ENSP00000245907.4:p.Gly906=
ENST00000245907.10:c.2716G=	ENSP00000245907.4:p.Gly906=
ENST00000594005.1:n.292G=
NM_000064.3:c.2716G=	NP_000055.2:p.Gly906=
NM_000064.4:c.2716G= MANE Select	NP_000055.2:p.Gly906=