Canonical Allele Identifier: CA2320550436

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679477G= , CM000681.2:g.6679477G=	GRCh38
NC_000019.9:g.6679488G= , CM000681.1:g.6679488G=	GRCh37
NC_000019.8:g.6630488G=	NCBI36
NG_009557.1:g.46175C= , LRG_27:g.46175C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2824C=
ENST00000695653.1:c.2385C=	ENSP00000512084.1:p.Phe795=
ENST00000695654.1:c.3501C=	ENSP00000512085.1:p.Phe1167=
ENST00000695689.1:c.447C=	ENSP00000512101.1:n.447C=
ENST00000695690.1:n.1541C=
ENST00000695691.1:n.1337C=
ENST00000245907.11:c.4476C= MANE Select	ENSP00000245907.4:p.Phe1492=
ENST00000245907.10:c.4476C=	ENSP00000245907.4:p.Phe1492=
ENST00000599668.1:n.71C=
ENST00000599899.5:n.1435C=
ENST00000601008.1:c.242-1519C=	ENSP00000471384.1:n.242-1519C=
NM_000064.3:c.4476C=	NP_000055.2:p.Phe1492=
NM_000064.4:c.4476C= MANE Select	NP_000055.2:p.Phe1492=