Canonical Allele Identifier: CA2320559057

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697428C= , CM000681.2:g.6697428C=	GRCh38
NC_000019.9:g.6697439C= , CM000681.1:g.6697439C=	GRCh37
NC_000019.8:g.6648439C=	NCBI36
NG_009557.1:g.28224G= , LRG_27:g.28224G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1060G=
ENST00000695652.1:c.2589G=	ENSP00000512083.1:p.Lys863=
ENST00000695653.1:c.621G=	ENSP00000512084.1:p.Lys207=
ENST00000695654.1:c.1836G=	ENSP00000512085.1:p.Lys612=
ENST00000695655.1:c.1653G=	ENSP00000512086.1:n.1653G=
ENST00000695692.1:n.2076G=
ENST00000245907.11:c.2712G= MANE Select	ENSP00000245907.4:p.Lys904=
ENST00000245907.10:c.2712G=	ENSP00000245907.4:p.Lys904=
ENST00000594005.1:n.288G=
NM_000064.3:c.2712G=	NP_000055.2:p.Lys904=
NM_000064.4:c.2712G= MANE Select	NP_000055.2:p.Lys904=