Canonical Allele Identifier: CA2320568376

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714019T= , CM000681.2:g.6714019T=	GRCh38
NC_000019.9:g.6714030T= , CM000681.1:g.6714030T=	GRCh37
NC_000019.8:g.6665030T=	NCBI36
NG_009557.1:g.11633A= , LRG_27:g.11633A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.623A=	ENSP00000512083.1:p.Lys208=
ENST00000245907.11:c.746A= MANE Select	ENSP00000245907.4:p.Lys249=
ENST00000245907.10:c.746A=	ENSP00000245907.4:p.Lys249=
ENST00000595577.1:n.250A=
NM_000064.3:c.746A=	NP_000055.2:p.Lys249=
NM_000064.4:c.746A= MANE Select	NP_000055.2:p.Lys249=