Canonical Allele Identifier: CA2320568526

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714307G= , CM000681.2:g.6714307G=	GRCh38
NC_000019.9:g.6714318G= , CM000681.1:g.6714318G=	GRCh37
NC_000019.8:g.6665318G=	NCBI36
NG_009557.1:g.11345C= , LRG_27:g.11345C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.476+45C=	ENSP00000512083.1:n.476+45C=
ENST00000245907.11:c.599+45C= MANE Select	ENSP00000245907.4:n.599+45C=
ENST00000245907.10:c.599+45C=	ENSP00000245907.4:n.599+45C=
ENST00000595577.1:n.45C=
NM_000064.3:c.599+45C=	NP_000055.2:n.599+45C=
NM_000064.4:c.599+45C= MANE Select	NP_000055.2:n.599+45C=