Canonical Allele Identifier: CA2320553470

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686212A= , CM000681.2:g.6686212A=	GRCh38
NC_000019.9:g.6686223A= , CM000681.1:g.6686223A=	GRCh37
NC_000019.8:g.6637223A=	NCBI36
NG_009557.1:g.39440T= , LRG_27:g.39440T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2070T=
ENST00000695652.1:c.3599T=	ENSP00000512083.1:p.Leu1200=
ENST00000695653.1:c.1631T=	ENSP00000512084.1:p.Leu544=
ENST00000695654.1:c.2747T=	ENSP00000512085.1:p.Leu916=
ENST00000695655.1:c.2663T=	ENSP00000512086.1:n.2663T=
ENST00000695692.1:n.3086T=
ENST00000245907.11:c.3722T= MANE Select	ENSP00000245907.4:p.Leu1241=
ENST00000245907.10:c.3722T=	ENSP00000245907.4:p.Leu1241=
ENST00000596238.1:n.165T=
ENST00000601008.1:c.241+534T=	ENSP00000471384.1:n.241+534T=
NM_000064.3:c.3722T=	NP_000055.2:p.Leu1241=
NM_000064.4:c.3722T= MANE Select	NP_000055.2:p.Leu1241=