Canonical Allele Identifier: CA2320570630

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6718339G= , CM000681.2:g.6718339G=	GRCh38
NC_000019.9:g.6718350G= , CM000681.1:g.6718350G=	GRCh37
NC_000019.8:g.6669350G=	NCBI36
NG_009557.1:g.7313C= , LRG_27:g.7313C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000594936.2:n.402C=
ENST00000695652.1:c.218C=	ENSP00000512083.1:p.Thr73=
ENST00000695693.1:c.341C=	ENSP00000512104.1:p.Thr114=
ENST00000245907.11:c.341C= MANE Select	ENSP00000245907.4:p.Thr114=
ENST00000245907.10:c.341C=	ENSP00000245907.4:p.Thr114=
ENST00000594936.1:n.402C=
ENST00000600744.1:c.218C=	ENSP00000472044.1:p.Thr73=
NM_000064.3:c.341C=	NP_000055.2:p.Thr114=
NM_000064.4:c.341C= MANE Select	NP_000055.2:p.Thr114=