Canonical Allele Identifier: CA2320551538

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681966T= , CM000681.2:g.6681966T=	GRCh38
NC_000019.9:g.6681977T= , CM000681.1:g.6681977T=	GRCh37
NC_000019.8:g.6632977T=	NCBI36
NG_009557.1:g.43686A= , LRG_27:g.43686A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2673A=
ENST00000695653.1:c.2234A=	ENSP00000512084.1:p.Asn745=
ENST00000695654.1:c.3350A=	ENSP00000512085.1:p.Asn1117=
ENST00000695689.1:c.296A=	ENSP00000512101.1:n.296A=
ENST00000695690.1:n.516A=
ENST00000695691.1:n.516A=
ENST00000245907.11:c.4325A= MANE Select	ENSP00000245907.4:p.Asn1442=
ENST00000245907.10:c.4325A=	ENSP00000245907.4:p.Asn1442=
ENST00000596548.1:c.446A=	ENSP00000469744.1:p.Asn149=
ENST00000599899.5:n.1284A=
ENST00000601008.1:c.242-4008A=	ENSP00000471384.1:n.242-4008A=
NM_000064.3:c.4325A=	NP_000055.2:p.Asn1442=
NM_000064.4:c.4325A= MANE Select	NP_000055.2:p.Asn1442=