Canonical Allele Identifier: CA2320568668

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714630G= , CM000681.2:g.6714630G=	GRCh38
NC_000019.9:g.6714641G= , CM000681.1:g.6714641G=	GRCh37
NC_000019.8:g.6665641G=	NCBI36
NG_009557.1:g.11022C= , LRG_27:g.11022C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.382-184C=	ENSP00000512083.1:n.382-184C=
ENST00000245907.11:c.505-184C= MANE Select	ENSP00000245907.4:n.505-184C=
ENST00000245907.10:c.505-184C=	ENSP00000245907.4:n.505-184C=
NM_000064.3:c.505-184C=	NP_000055.2:n.505-184C=
NM_000064.4:c.505-184C= MANE Select	NP_000055.2:n.505-184C=