Canonical Allele Identifier: CA2320568373

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714007A= , CM000681.2:g.6714007A=	GRCh38
NC_000019.9:g.6714018A= , CM000681.1:g.6714018A=	GRCh37
NC_000019.8:g.6665018A=	NCBI36
NG_009557.1:g.11645T= , LRG_27:g.11645T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.635T=	ENSP00000512083.1:p.Val212=
ENST00000245907.11:c.758T= MANE Select	ENSP00000245907.4:p.Val253=
ENST00000245907.10:c.758T=	ENSP00000245907.4:p.Val253=
ENST00000595577.1:n.262T=
NM_000064.3:c.758T=	NP_000055.2:p.Val253=
NM_000064.4:c.758T= MANE Select	NP_000055.2:p.Val253=