Canonical Allele Identifier: CA2320568675

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714636C= , CM000681.2:g.6714636C=	GRCh38
NC_000019.9:g.6714647C= , CM000681.1:g.6714647C=	GRCh37
NC_000019.8:g.6665647C=	NCBI36
NG_009557.1:g.11016G= , LRG_27:g.11016G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.382-190G=	ENSP00000512083.1:n.382-190G=
ENST00000245907.11:c.505-190G= MANE Select	ENSP00000245907.4:n.505-190G=
ENST00000245907.10:c.505-190G=	ENSP00000245907.4:n.505-190G=
NM_000064.3:c.505-190G=	NP_000055.2:n.505-190G=
NM_000064.4:c.505-190G= MANE Select	NP_000055.2:n.505-190G=