Canonical Allele Identifier: CA2320568162

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713772C= , CM000681.2:g.6713772C=	GRCh38
NC_000019.9:g.6713783C= , CM000681.1:g.6713783C=	GRCh37
NC_000019.8:g.6664783C=	NCBI36
NG_009557.1:g.11880G= , LRG_27:g.11880G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.650+220G=	ENSP00000512083.1:n.650+220G=
ENST00000245907.11:c.773+220G= MANE Select	ENSP00000245907.4:n.773+220G=
ENST00000245907.10:c.773+220G=	ENSP00000245907.4:n.773+220G=
ENST00000595577.1:n.277+220G=
ENST00000597442.5:n.17G=
NM_000064.3:c.773+220G=	NP_000055.2:n.773+220G=
NM_000064.4:c.773+220G= MANE Select	NP_000055.2:n.773+220G=