Canonical Allele Identifier: CA2320568461

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714201T= , CM000681.2:g.6714201T=	GRCh38
NC_000019.9:g.6714212T= , CM000681.1:g.6714212T=	GRCh37
NC_000019.8:g.6665212T=	NCBI36
NG_009557.1:g.11451A= , LRG_27:g.11451A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.524A=	ENSP00000512083.1:p.Gln175=
ENST00000245907.11:c.647A= MANE Select	ENSP00000245907.4:p.Gln216=
ENST00000245907.10:c.647A=	ENSP00000245907.4:p.Gln216=
ENST00000595577.1:n.151A=
NM_000064.3:c.647A=	NP_000055.2:p.Gln216=
NM_000064.4:c.647A= MANE Select	NP_000055.2:p.Gln216=