Canonical Allele Identifier: CA2320568492

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714269T= , CM000681.2:g.6714269T=	GRCh38
NC_000019.9:g.6714280T= , CM000681.1:g.6714280T=	GRCh37
NC_000019.8:g.6665280T=	NCBI36
NG_009557.1:g.11383A= , LRG_27:g.11383A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.477-21A=	ENSP00000512083.1:n.477-21A=
ENST00000245907.11:c.600-21A= MANE Select	ENSP00000245907.4:n.600-21A=
ENST00000245907.10:c.600-21A=	ENSP00000245907.4:n.600-21A=
ENST00000595577.1:n.83A=
NM_000064.3:c.600-21A=	NP_000055.2:n.600-21A=
NM_000064.4:c.600-21A= MANE Select	NP_000055.2:n.600-21A=