Canonical Allele Identifier: CA2320551942

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682989C= , CM000681.2:g.6682989C=	GRCh38
NC_000019.9:g.6683000C= , CM000681.1:g.6683000C=	GRCh37
NC_000019.8:g.6634000C=	NCBI36
NG_009557.1:g.42663G= , LRG_27:g.42663G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2521-760G=
ENST00000695653.1:c.2082-760G=	ENSP00000512084.1:n.2082-760G=
ENST00000695654.1:c.3198-760G=	ENSP00000512085.1:n.3198-760G=
ENST00000695689.1:c.84-323G=	ENSP00000512101.1:n.84-323G=
ENST00000695690.1:n.364-760G=
ENST00000695691.1:n.364-760G=
ENST00000245907.11:c.4173-760G= MANE Select	ENSP00000245907.4:n.4173-760G=
ENST00000245907.10:c.4173-760G=	ENSP00000245907.4:n.4173-760G=
ENST00000596548.1:c.294-760G=	ENSP00000469744.1:n.294-760G=
ENST00000599899.5:n.372G=
ENST00000601008.1:c.241+3757G=	ENSP00000471384.1:n.241+3757G=
NM_000064.3:c.4173-760G=	NP_000055.2:n.4173-760G=
NM_000064.4:c.4173-760G= MANE Select	NP_000055.2:n.4173-760G=