Canonical Allele Identifier: CA2320568393

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714077G= , CM000681.2:g.6714077G=	GRCh38
NC_000019.9:g.6714088G= , CM000681.1:g.6714088G=	GRCh37
NC_000019.8:g.6665088G=	NCBI36
NG_009557.1:g.11575C= , LRG_27:g.11575C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.565C=	ENSP00000512083.1:p.Pro189=
ENST00000245907.11:c.688C= MANE Select	ENSP00000245907.4:p.Pro230=
ENST00000245907.10:c.688C=	ENSP00000245907.4:p.Pro230=
ENST00000595577.1:n.192C=
NM_000064.3:c.688C=	NP_000055.2:p.Pro230=
NM_000064.4:c.688C= MANE Select	NP_000055.2:p.Pro230=