Canonical Allele Identifier: CA2320568496

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714272T= , CM000681.2:g.6714272T=	GRCh38
NC_000019.9:g.6714283T= , CM000681.1:g.6714283T=	GRCh37
NC_000019.8:g.6665283T=	NCBI36
NG_009557.1:g.11380A= , LRG_27:g.11380A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.477-24A=	ENSP00000512083.1:n.477-24A=
ENST00000245907.11:c.600-24A= MANE Select	ENSP00000245907.4:n.600-24A=
ENST00000245907.10:c.600-24A=	ENSP00000245907.4:n.600-24A=
ENST00000595577.1:n.80A=
NM_000064.3:c.600-24A=	NP_000055.2:n.600-24A=
NM_000064.4:c.600-24A= MANE Select	NP_000055.2:n.600-24A=