Canonical Allele Identifier: CA2320561816

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6701501C= , CM000681.2:g.6701501C=	GRCh38
NC_000019.9:g.6701512C= , CM000681.1:g.6701512C=	GRCh37
NC_000019.8:g.6652512C=	NCBI36
NG_009557.1:g.24151G= , LRG_27:g.24151G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.788+626G=
ENST00000695652.1:c.2317+626G=	ENSP00000512083.1:n.2317+626G=
ENST00000695653.1:c.349+626G=	ENSP00000512084.1:n.349+626G=
ENST00000695654.1:c.1564+626G=	ENSP00000512085.1:n.1564+626G=
ENST00000695655.1:c.1381+626G=	ENSP00000512086.1:n.1381+626G=
ENST00000695692.1:n.1804+626G=
ENST00000245907.11:c.2440+626G= MANE Select	ENSP00000245907.4:n.2440+626G=
ENST00000245907.10:c.2440+626G=	ENSP00000245907.4:n.2440+626G=
ENST00000602053.1:n.488+626G=
NM_000064.3:c.2440+626G=	NP_000055.2:n.2440+626G=
NM_000064.4:c.2440+626G= MANE Select	NP_000055.2:n.2440+626G=