Canonical Allele Identifier: CA2320555666

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6690475C= , CM000681.2:g.6690475C=	GRCh38
NC_000019.9:g.6690486C= , CM000681.1:g.6690486C=	GRCh37
NC_000019.8:g.6641486C=	NCBI36
NG_009557.1:g.35177G= , LRG_27:g.35177G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.1837+154G=
ENST00000695652.1:c.3366+154G=	ENSP00000512083.1:n.3366+154G=
ENST00000695653.1:c.1398+154G=	ENSP00000512084.1:n.1398+154G=
ENST00000695654.1:c.2514+2449G=	ENSP00000512085.1:n.2514+2449G=
ENST00000695655.1:c.2430+154G=	ENSP00000512086.1:n.2430+154G=
ENST00000695692.1:n.2853+154G=
ENST00000245907.11:c.3489+154G= MANE Select	ENSP00000245907.4:n.3489+154G=
ENST00000245907.10:c.3489+154G=	ENSP00000245907.4:n.3489+154G=
ENST00000598805.2:n.259+154G=
ENST00000601008.1:c.84+154G=	ENSP00000471384.1:n.84+154G=
NM_000064.3:c.3489+154G=	NP_000055.2:n.3489+154G=
NM_000064.4:c.3489+154G= MANE Select	NP_000055.2:n.3489+154G=