Canonical Allele Identifier: CA2320565968

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709836C= , CM000681.2:g.6709836C=	GRCh38
NC_000019.9:g.6709847C= , CM000681.1:g.6709847C=	GRCh37
NC_000019.8:g.6660847C=	NCBI36
NG_009557.1:g.15816G= , LRG_27:g.15816G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1570G=	ENSP00000512083.1:p.Val524=
ENST00000695654.1:c.817G=	ENSP00000512085.1:p.Val273=
ENST00000695655.1:c.634G=	ENSP00000512086.1:n.634G=
ENST00000695692.1:n.1057G=
ENST00000245907.11:c.1693G= MANE Select	ENSP00000245907.4:p.Val565=
ENST00000245907.10:c.1693G=	ENSP00000245907.4:p.Val565=
ENST00000600763.1:n.326G=
NM_000064.3:c.1693G=	NP_000055.2:p.Val565=
NM_000064.4:c.1693G= MANE Select	NP_000055.2:p.Val565=