Canonical Allele Identifier: CA2320567943

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713470G= , CM000681.2:g.6713470G=	GRCh38
NC_000019.9:g.6713481G= , CM000681.1:g.6713481G=	GRCh37
NC_000019.8:g.6664481G=	NCBI36
NG_009557.1:g.12182C= , LRG_27:g.12182C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.690C=	ENSP00000512083.1:p.Val230=
ENST00000695692.1:n.137C=
ENST00000245907.11:c.813C= MANE Select	ENSP00000245907.4:p.Val271=
ENST00000245907.10:c.813C=	ENSP00000245907.4:p.Val271=
ENST00000595577.1:n.317C=
ENST00000597442.5:n.63C=
NM_000064.3:c.813C=	NP_000055.2:p.Val271=
NM_000064.4:c.813C= MANE Select	NP_000055.2:p.Val271=