Canonical Allele Identifier: CA2320565964

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709825G= , CM000681.2:g.6709825G=	GRCh38
NC_000019.9:g.6709836G= , CM000681.1:g.6709836G=	GRCh37
NC_000019.8:g.6660836G=	NCBI36
NG_009557.1:g.15827C= , LRG_27:g.15827C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1581C=	ENSP00000512083.1:p.Gly527=
ENST00000695654.1:c.828C=	ENSP00000512085.1:p.Gly276=
ENST00000695655.1:c.645C=	ENSP00000512086.1:n.645C=
ENST00000695692.1:n.1068C=
ENST00000245907.11:c.1704C= MANE Select	ENSP00000245907.4:p.Gly568=
ENST00000245907.10:c.1704C=	ENSP00000245907.4:p.Gly568=
ENST00000600763.1:n.337C=
NM_000064.3:c.1704C=	NP_000055.2:p.Gly568=
NM_000064.4:c.1704C= MANE Select	NP_000055.2:p.Gly568=