Canonical Allele Identifier: CA2320570610

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6718280T= , CM000681.2:g.6718280T=	GRCh38
NC_000019.9:g.6718291T= , CM000681.1:g.6718291T=	GRCh37
NC_000019.8:g.6669291T=	NCBI36
NG_009557.1:g.7372A= , LRG_27:g.7372A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594936.2:n.461A=
ENST00000695652.1:c.277A=	ENSP00000512083.1:p.Thr93=
ENST00000695693.1:c.400A=	ENSP00000512104.1:p.Thr134=
ENST00000245907.11:c.400A= MANE Select	ENSP00000245907.4:p.Thr134=
ENST00000245907.10:c.400A=	ENSP00000245907.4:p.Thr134=
ENST00000594936.1:n.461A=
ENST00000600744.1:c.277A=	ENSP00000472044.1:p.Thr93=
NM_000064.3:c.400A=	NP_000055.2:p.Thr134=
NM_000064.4:c.400A= MANE Select	NP_000055.2:p.Thr134=