Canonical Allele Identifier: CA2320553363

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685999T= , CM000681.2:g.6685999T=	GRCh38
NC_000019.9:g.6686010T= , CM000681.1:g.6686010T=	GRCh37
NC_000019.8:g.6637010T=	NCBI36
NG_009557.1:g.39653A= , LRG_27:g.39653A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2158+125A=
ENST00000695653.1:c.1719+125A=	ENSP00000512084.1:n.1719+125A=
ENST00000695654.1:c.2835+125A=	ENSP00000512085.1:n.2835+125A=
ENST00000245907.11:c.3810+125A= MANE Select	ENSP00000245907.4:n.3810+125A=
ENST00000245907.10:c.3810+125A=	ENSP00000245907.4:n.3810+125A=
ENST00000596238.1:n.253+125A=
ENST00000601008.1:c.241+747A=	ENSP00000471384.1:n.241+747A=
NM_000064.3:c.3810+125A=	NP_000055.2:n.3810+125A=
NM_000064.4:c.3810+125A= MANE Select	NP_000055.2:n.3810+125A=