Canonical Allele Identifier: CA2320555653

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6690447G= , CM000681.2:g.6690447G=	GRCh38
NC_000019.9:g.6690458G= , CM000681.1:g.6690458G=	GRCh37
NC_000019.8:g.6641458G=	NCBI36
NG_009557.1:g.35205C= , LRG_27:g.35205C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.1837+182C=
ENST00000695652.1:c.3366+182C=	ENSP00000512083.1:n.3366+182C=
ENST00000695653.1:c.1398+182C=	ENSP00000512084.1:n.1398+182C=
ENST00000695654.1:c.2514+2477C=	ENSP00000512085.1:n.2514+2477C=
ENST00000695655.1:c.2430+182C=	ENSP00000512086.1:n.2430+182C=
ENST00000695692.1:n.2853+182C=
ENST00000245907.11:c.3489+182C= MANE Select	ENSP00000245907.4:n.3489+182C=
ENST00000245907.10:c.3489+182C=	ENSP00000245907.4:n.3489+182C=
ENST00000598805.2:n.259+182C=
ENST00000601008.1:c.84+182C=	ENSP00000471384.1:n.84+182C=
NM_000064.3:c.3489+182C=	NP_000055.2:n.3489+182C=
NM_000064.4:c.3489+182C= MANE Select	NP_000055.2:n.3489+182C=