Canonical Allele Identifier: CA2320567938

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713460T= , CM000681.2:g.6713460T=	GRCh38
NC_000019.9:g.6713471T= , CM000681.1:g.6713471T=	GRCh37
NC_000019.8:g.6664471T=	NCBI36
NG_009557.1:g.12192A= , LRG_27:g.12192A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.700A=	ENSP00000512083.1:p.Ile234=
ENST00000695692.1:n.147A=
ENST00000245907.11:c.823A= MANE Select	ENSP00000245907.4:p.Ile275=
ENST00000245907.10:c.823A=	ENSP00000245907.4:p.Ile275=
ENST00000595577.1:n.327A=
ENST00000597442.5:n.73A=
NM_000064.3:c.823A=	NP_000055.2:p.Ile275=
NM_000064.4:c.823A= MANE Select	NP_000055.2:p.Ile275=