Canonical Allele Identifier: CA2320551562

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682026G= , CM000681.2:g.6682026G=	GRCh38
NC_000019.9:g.6682037G= , CM000681.1:g.6682037G=	GRCh37
NC_000019.8:g.6633037G=	NCBI36
NG_009557.1:g.43626C= , LRG_27:g.43626C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2613C=
ENST00000695653.1:c.2174C=	ENSP00000512084.1:p.Ala725=
ENST00000695654.1:c.3290C=	ENSP00000512085.1:p.Ala1097=
ENST00000695689.1:c.236C=	ENSP00000512101.1:n.236C=
ENST00000695690.1:n.456C=
ENST00000695691.1:n.456C=
ENST00000245907.11:c.4265C= MANE Select	ENSP00000245907.4:p.Ala1422=
ENST00000245907.10:c.4265C=	ENSP00000245907.4:p.Ala1422=
ENST00000596548.1:c.386C=	ENSP00000469744.1:p.Ala129=
ENST00000599899.5:n.1224C=
ENST00000601008.1:c.242-4068C=	ENSP00000471384.1:n.242-4068C=
NM_000064.3:c.4265C=	NP_000055.2:p.Ala1422=
NM_000064.4:c.4265C= MANE Select	NP_000055.2:p.Ala1422=