Canonical Allele Identifier: CA2320568546

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714357G= , CM000681.2:g.6714357G=	GRCh38
NC_000019.9:g.6714368G= , CM000681.1:g.6714368G=	GRCh37
NC_000019.8:g.6665368G=	NCBI36
NG_009557.1:g.11295C= , LRG_27:g.11295C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.471C=	ENSP00000512083.1:p.Leu157=
ENST00000245907.11:c.594C= MANE Select	ENSP00000245907.4:p.Leu198=
ENST00000245907.10:c.594C=	ENSP00000245907.4:p.Leu198=
NM_000064.3:c.594C=	NP_000055.2:p.Leu198=
NM_000064.4:c.594C= MANE Select	NP_000055.2:p.Leu198=