Canonical Allele Identifier: CA2320567838

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713248C= , CM000681.2:g.6713248C=	GRCh38
NC_000019.9:g.6713259C= , CM000681.1:g.6713259C=	GRCh37
NC_000019.8:g.6664259C=	NCBI36
NG_009557.1:g.12404G= , LRG_27:g.12404G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.821G=	ENSP00000512083.1:p.Arg274=
ENST00000695654.1:c.68G=	ENSP00000512085.1:p.Arg23=
ENST00000695692.1:n.268G=
ENST00000245907.11:c.944G= MANE Select	ENSP00000245907.4:p.Arg315=
ENST00000245907.10:c.944G=	ENSP00000245907.4:p.Arg315=
ENST00000594270.5:n.68G=
ENST00000595577.1:n.448G=
ENST00000597442.5:n.194G=
NM_000064.3:c.944G=	NP_000055.2:p.Arg315=
NM_000064.4:c.944G= MANE Select	NP_000055.2:p.Arg315=