Canonical Allele Identifier: CA2320559046

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697394C= , CM000681.2:g.6697394C=	GRCh38
NC_000019.9:g.6697405C= , CM000681.1:g.6697405C=	GRCh37
NC_000019.8:g.6648405C=	NCBI36
NG_009557.1:g.28258G= , LRG_27:g.28258G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1094G=
ENST00000695652.1:c.2623G=	ENSP00000512083.1:p.Val875=
ENST00000695653.1:c.655G=	ENSP00000512084.1:p.Val219=
ENST00000695654.1:c.1870G=	ENSP00000512085.1:p.Val624=
ENST00000695655.1:c.1687G=	ENSP00000512086.1:n.1687G=
ENST00000695692.1:n.2110G=
ENST00000245907.11:c.2746G= MANE Select	ENSP00000245907.4:p.Val916=
ENST00000245907.10:c.2746G=	ENSP00000245907.4:p.Val916=
ENST00000594005.1:n.322G=
NM_000064.3:c.2746G=	NP_000055.2:p.Val916=
NM_000064.4:c.2746G= MANE Select	NP_000055.2:p.Val916=