Canonical Allele Identifier: CA2320567933

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713449G= , CM000681.2:g.6713449G=	GRCh38
NC_000019.9:g.6713460G= , CM000681.1:g.6713460G=	GRCh37
NC_000019.8:g.6664460G=	NCBI36
NG_009557.1:g.12203C= , LRG_27:g.12203C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.711C=	ENSP00000512083.1:p.Gly237=
ENST00000695692.1:n.158C=
ENST00000245907.11:c.834C= MANE Select	ENSP00000245907.4:p.Gly278=
ENST00000245907.10:c.834C=	ENSP00000245907.4:p.Gly278=
ENST00000595577.1:n.338C=
ENST00000597442.5:n.84C=
NM_000064.3:c.834C=	NP_000055.2:p.Gly278=
NM_000064.4:c.834C= MANE Select	NP_000055.2:p.Gly278=