Canonical Allele Identifier: CA2320559175

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697676A= , CM000681.2:g.6697676A=	GRCh38
NC_000019.9:g.6697687A= , CM000681.1:g.6697687A=	GRCh37
NC_000019.8:g.6648687A=	NCBI36
NG_009557.1:g.27976T= , LRG_27:g.27976T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.907T=
ENST00000695652.1:c.2436T=	ENSP00000512083.1:p.Asn812=
ENST00000695653.1:c.468T=	ENSP00000512084.1:p.Asn156=
ENST00000695654.1:c.1683T=	ENSP00000512085.1:p.Asn561=
ENST00000695655.1:c.1500T=	ENSP00000512086.1:n.1500T=
ENST00000695692.1:n.1923T=
ENST00000245907.11:c.2559T= MANE Select	ENSP00000245907.4:p.Asn853=
ENST00000245907.10:c.2559T=	ENSP00000245907.4:p.Asn853=
ENST00000594005.1:n.40T=
ENST00000602053.1:n.607T=
NM_000064.3:c.2559T=	NP_000055.2:p.Asn853=
NM_000064.4:c.2559T= MANE Select	NP_000055.2:p.Asn853=