Canonical Allele Identifier: CA2320553474

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686227G= , CM000681.2:g.6686227G=	GRCh38
NC_000019.9:g.6686238G= , CM000681.1:g.6686238G=	GRCh37
NC_000019.8:g.6637238G=	NCBI36
NG_009557.1:g.39425C= , LRG_27:g.39425C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2055C=
ENST00000695652.1:c.3584C=	ENSP00000512083.1:p.Ala1195=
ENST00000695653.1:c.1616C=	ENSP00000512084.1:p.Ala539=
ENST00000695654.1:c.2732C=	ENSP00000512085.1:p.Ala911=
ENST00000695655.1:c.2648C=	ENSP00000512086.1:n.2648C=
ENST00000695692.1:n.3071C=
ENST00000245907.11:c.3707C= MANE Select	ENSP00000245907.4:p.Ala1236=
ENST00000245907.10:c.3707C=	ENSP00000245907.4:p.Ala1236=
ENST00000596238.1:n.150C=
ENST00000601008.1:c.241+519C=	ENSP00000471384.1:n.241+519C=
NM_000064.3:c.3707C=	NP_000055.2:p.Ala1236=
NM_000064.4:c.3707C= MANE Select	NP_000055.2:p.Ala1236=