Canonical Allele Identifier: CA2320567964

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713533T= , CM000681.2:g.6713533T=	GRCh38
NC_000019.9:g.6713544T= , CM000681.1:g.6713544T=	GRCh37
NC_000019.8:g.6664544T=	NCBI36
NG_009557.1:g.12119A= , LRG_27:g.12119A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-24A=	ENSP00000512083.1:n.651-24A=
ENST00000695692.1:n.74A=
ENST00000245907.11:c.774-24A= MANE Select	ENSP00000245907.4:n.774-24A=
ENST00000245907.10:c.774-24A=	ENSP00000245907.4:n.774-24A=
ENST00000595577.1:n.278-24A=
ENST00000597442.5:n.24-24A=
NM_000064.3:c.774-24A=	NP_000055.2:n.774-24A=
NM_000064.4:c.774-24A= MANE Select	NP_000055.2:n.774-24A=