Canonical Allele Identifier: CA2320568500

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714277C= , CM000681.2:g.6714277C=	GRCh38
NC_000019.9:g.6714288C= , CM000681.1:g.6714288C=	GRCh37
NC_000019.8:g.6665288C=	NCBI36
NG_009557.1:g.11375G= , LRG_27:g.11375G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.477-29G=	ENSP00000512083.1:n.477-29G=
ENST00000245907.11:c.600-29G= MANE Select	ENSP00000245907.4:n.600-29G=
ENST00000245907.10:c.600-29G=	ENSP00000245907.4:n.600-29G=
ENST00000595577.1:n.75G=
NM_000064.3:c.600-29G=	NP_000055.2:n.600-29G=
NM_000064.4:c.600-29G= MANE Select	NP_000055.2:n.600-29G=