Canonical Allele Identifier: CA2320559190

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697709G= , CM000681.2:g.6697709G=	GRCh38
NC_000019.9:g.6697720G= , CM000681.1:g.6697720G=	GRCh37
NC_000019.8:g.6648720G=	NCBI36
NG_009557.1:g.27943C= , LRG_27:g.27943C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.874C=
ENST00000695652.1:c.2403C=	ENSP00000512083.1:p.Asn801=
ENST00000695653.1:c.435C=	ENSP00000512084.1:p.Asn145=
ENST00000695654.1:c.1650C=	ENSP00000512085.1:p.Asn550=
ENST00000695655.1:c.1467C=	ENSP00000512086.1:n.1467C=
ENST00000695692.1:n.1890C=
ENST00000245907.11:c.2526C= MANE Select	ENSP00000245907.4:p.Asn842=
ENST00000245907.10:c.2526C=	ENSP00000245907.4:p.Asn842=
ENST00000594005.1:n.7C=
ENST00000602053.1:n.574C=
NM_000064.3:c.2526C=	NP_000055.2:p.Asn842=
NM_000064.4:c.2526C= MANE Select	NP_000055.2:p.Asn842=