Canonical Allele Identifier: CA2320553479

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686236G= , CM000681.2:g.6686236G=	GRCh38
NC_000019.9:g.6686247G= , CM000681.1:g.6686247G=	GRCh37
NC_000019.8:g.6637247G=	NCBI36
NG_009557.1:g.39416C= , LRG_27:g.39416C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2046C=
ENST00000695652.1:c.3575C=	ENSP00000512083.1:p.Thr1192=
ENST00000695653.1:c.1607C=	ENSP00000512084.1:p.Thr536=
ENST00000695654.1:c.2723C=	ENSP00000512085.1:p.Thr908=
ENST00000695655.1:c.2639C=	ENSP00000512086.1:n.2639C=
ENST00000695692.1:n.3062C=
ENST00000245907.11:c.3698C= MANE Select	ENSP00000245907.4:p.Thr1233=
ENST00000245907.10:c.3698C=	ENSP00000245907.4:p.Thr1233=
ENST00000596238.1:n.141C=
ENST00000601008.1:c.241+510C=	ENSP00000471384.1:n.241+510C=
NM_000064.3:c.3698C=	NP_000055.2:p.Thr1233=
NM_000064.4:c.3698C= MANE Select	NP_000055.2:p.Thr1233=