Canonical Allele Identifier: CA2320553476

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686230T= , CM000681.2:g.6686230T=	GRCh38
NC_000019.9:g.6686241T= , CM000681.1:g.6686241T=	GRCh37
NC_000019.8:g.6637241T=	NCBI36
NG_009557.1:g.39422A= , LRG_27:g.39422A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2052A=
ENST00000695652.1:c.3581A=	ENSP00000512083.1:p.Tyr1194=
ENST00000695653.1:c.1613A=	ENSP00000512084.1:p.Tyr538=
ENST00000695654.1:c.2729A=	ENSP00000512085.1:p.Tyr910=
ENST00000695655.1:c.2645A=	ENSP00000512086.1:n.2645A=
ENST00000695692.1:n.3068A=
ENST00000245907.11:c.3704A= MANE Select	ENSP00000245907.4:p.Tyr1235=
ENST00000245907.10:c.3704A=	ENSP00000245907.4:p.Tyr1235=
ENST00000596238.1:n.147A=
ENST00000601008.1:c.241+516A=	ENSP00000471384.1:n.241+516A=
NM_000064.3:c.3704A=	NP_000055.2:p.Tyr1235=
NM_000064.4:c.3704A= MANE Select	NP_000055.2:p.Tyr1235=