Canonical Allele Identifier: CA2320551716

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682358A= , CM000681.2:g.6682358A=	GRCh38
NC_000019.9:g.6682369A= , CM000681.1:g.6682369A=	GRCh37
NC_000019.8:g.6633369A=	NCBI36
NG_009557.1:g.43294T= , LRG_27:g.43294T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2521-129T=
ENST00000695653.1:c.2082-129T=	ENSP00000512084.1:n.2082-129T=
ENST00000695654.1:c.3198-129T=	ENSP00000512085.1:n.3198-129T=
ENST00000695689.1:c.144-129T=	ENSP00000512101.1:n.144-129T=
ENST00000695690.1:n.364-129T=
ENST00000695691.1:n.364-129T=
ENST00000245907.11:c.4173-129T= MANE Select	ENSP00000245907.4:n.4173-129T=
ENST00000245907.10:c.4173-129T=	ENSP00000245907.4:n.4173-129T=
ENST00000596548.1:c.294-129T=	ENSP00000469744.1:n.294-129T=
ENST00000599899.5:n.1003T=
ENST00000601008.1:c.241+4388T=	ENSP00000471384.1:n.241+4388T=
NM_000064.3:c.4173-129T=	NP_000055.2:n.4173-129T=
NM_000064.4:c.4173-129T= MANE Select	NP_000055.2:n.4173-129T=