Canonical Allele Identifier: CA2320568462

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714202G= , CM000681.2:g.6714202G=	GRCh38
NC_000019.9:g.6714213G= , CM000681.1:g.6714213G=	GRCh37
NC_000019.8:g.6665213G=	NCBI36
NG_009557.1:g.11450C= , LRG_27:g.11450C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.523C=	ENSP00000512083.1:p.Gln175=
ENST00000245907.11:c.646C= MANE Select	ENSP00000245907.4:p.Gln216=
ENST00000245907.10:c.646C=	ENSP00000245907.4:p.Gln216=
ENST00000595577.1:n.150C=
NM_000064.3:c.646C=	NP_000055.2:p.Gln216=
NM_000064.4:c.646C= MANE Select	NP_000055.2:p.Gln216=