Canonical Allele Identifier: CA2320568674

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714635G= , CM000681.2:g.6714635G=	GRCh38
NC_000019.9:g.6714646G= , CM000681.1:g.6714646G=	GRCh37
NC_000019.8:g.6665646G=	NCBI36
NG_009557.1:g.11017C= , LRG_27:g.11017C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.382-189C=	ENSP00000512083.1:n.382-189C=
ENST00000245907.11:c.505-189C= MANE Select	ENSP00000245907.4:n.505-189C=
ENST00000245907.10:c.505-189C=	ENSP00000245907.4:n.505-189C=
NM_000064.3:c.505-189C=	NP_000055.2:n.505-189C=
NM_000064.4:c.505-189C= MANE Select	NP_000055.2:n.505-189C=