Canonical Allele Identifier: CA2320551636

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682190G= , CM000681.2:g.6682190G=	GRCh38
NC_000019.9:g.6682201G= , CM000681.1:g.6682201G=	GRCh37
NC_000019.8:g.6633201G=	NCBI36
NG_009557.1:g.43462C= , LRG_27:g.43462C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2560C=
ENST00000695653.1:c.2121C=	ENSP00000512084.1:p.Asp707=
ENST00000695654.1:c.3237C=	ENSP00000512085.1:p.Asp1079=
ENST00000695689.1:c.183C=	ENSP00000512101.1:n.183C=
ENST00000695690.1:n.403C=
ENST00000695691.1:n.403C=
ENST00000245907.11:c.4212C= MANE Select	ENSP00000245907.4:p.Asp1404=
ENST00000245907.10:c.4212C=	ENSP00000245907.4:p.Asp1404=
ENST00000596548.1:c.333C=	ENSP00000469744.1:p.Asp111=
ENST00000599899.5:n.1171C=
ENST00000601008.1:c.242-4232C=	ENSP00000471384.1:n.242-4232C=
NM_000064.3:c.4212C=	NP_000055.2:p.Asp1404=
NM_000064.4:c.4212C= MANE Select	NP_000055.2:p.Asp1404=