Canonical Allele Identifier: CA2320568388

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714068C= , CM000681.2:g.6714068C=	GRCh38
NC_000019.9:g.6714079C= , CM000681.1:g.6714079C=	GRCh37
NC_000019.8:g.6665079C=	NCBI36
NG_009557.1:g.11584G= , LRG_27:g.11584G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.574G=	ENSP00000512083.1:p.Glu192=
ENST00000245907.11:c.697G= MANE Select	ENSP00000245907.4:p.Glu233=
ENST00000245907.10:c.697G=	ENSP00000245907.4:p.Glu233=
ENST00000595577.1:n.201G=
NM_000064.3:c.697G=	NP_000055.2:p.Glu233=
NM_000064.4:c.697G= MANE Select	NP_000055.2:p.Glu233=