Canonical Allele Identifier: CA2320551585

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682071C= , CM000681.2:g.6682071C=	GRCh38
NC_000019.9:g.6682082C= , CM000681.1:g.6682082C=	GRCh37
NC_000019.8:g.6633082C=	NCBI36
NG_009557.1:g.43581G= , LRG_27:g.43581G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2609-41G=
ENST00000695653.1:c.2170-41G=	ENSP00000512084.1:n.2170-41G=
ENST00000695654.1:c.3286-41G=	ENSP00000512085.1:n.3286-41G=
ENST00000695689.1:c.232-41G=	ENSP00000512101.1:n.232-41G=
ENST00000695690.1:n.452-41G=
ENST00000695691.1:n.452-41G=
ENST00000245907.11:c.4261-41G= MANE Select	ENSP00000245907.4:n.4261-41G=
ENST00000245907.10:c.4261-41G=	ENSP00000245907.4:n.4261-41G=
ENST00000596548.1:c.382-41G=	ENSP00000469744.1:n.382-41G=
ENST00000599899.5:n.1220-41G=
ENST00000601008.1:c.242-4113G=	ENSP00000471384.1:n.242-4113G=
NM_000064.3:c.4261-41G=	NP_000055.2:n.4261-41G=
NM_000064.4:c.4261-41G= MANE Select	NP_000055.2:n.4261-41G=