Canonical Allele Identifier: CA2320559056

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697427T= , CM000681.2:g.6697427T=	GRCh38
NC_000019.9:g.6697438T= , CM000681.1:g.6697438T=	GRCh37
NC_000019.8:g.6648438T=	NCBI36
NG_009557.1:g.28225A= , LRG_27:g.28225A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1061A=
ENST00000695652.1:c.2590A=	ENSP00000512083.1:p.Thr864=
ENST00000695653.1:c.622A=	ENSP00000512084.1:p.Thr208=
ENST00000695654.1:c.1837A=	ENSP00000512085.1:p.Thr613=
ENST00000695655.1:c.1654A=	ENSP00000512086.1:n.1654A=
ENST00000695692.1:n.2077A=
ENST00000245907.11:c.2713A= MANE Select	ENSP00000245907.4:p.Thr905=
ENST00000245907.10:c.2713A=	ENSP00000245907.4:p.Thr905=
ENST00000594005.1:n.289A=
NM_000064.3:c.2713A=	NP_000055.2:p.Thr905=
NM_000064.4:c.2713A= MANE Select	NP_000055.2:p.Thr905=