Canonical Allele Identifier: CA2320559096

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697505T= , CM000681.2:g.6697505T=	GRCh38
NC_000019.9:g.6697516T= , CM000681.1:g.6697516T=	GRCh37
NC_000019.8:g.6648516T=	NCBI36
NG_009557.1:g.28147A= , LRG_27:g.28147A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.983A=
ENST00000695652.1:c.2512A=	ENSP00000512083.1:p.Lys838=
ENST00000695653.1:c.544A=	ENSP00000512084.1:p.Lys182=
ENST00000695654.1:c.1759A=	ENSP00000512085.1:p.Lys587=
ENST00000695655.1:c.1576A=	ENSP00000512086.1:n.1576A=
ENST00000695692.1:n.1999A=
ENST00000245907.11:c.2635A= MANE Select	ENSP00000245907.4:p.Lys879=
ENST00000245907.10:c.2635A=	ENSP00000245907.4:p.Lys879=
ENST00000594005.1:n.211A=
NM_000064.3:c.2635A=	NP_000055.2:p.Lys879=
NM_000064.4:c.2635A= MANE Select	NP_000055.2:p.Lys879=