Canonical Allele Identifier: CA2320565986

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709888A= , CM000681.2:g.6709888A=	GRCh38
NC_000019.9:g.6709899A= , CM000681.1:g.6709899A=	GRCh37
NC_000019.8:g.6660899A=	NCBI36
NG_009557.1:g.15764T= , LRG_27:g.15764T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-46T=	ENSP00000512083.1:n.1564-46T=
ENST00000695654.1:c.811-46T=	ENSP00000512085.1:n.811-46T=
ENST00000695655.1:c.592-10T=	ENSP00000512086.1:n.592-10T=
ENST00000695692.1:n.1051-46T=
ENST00000245907.11:c.1687-46T= MANE Select	ENSP00000245907.4:n.1687-46T=
ENST00000245907.10:c.1687-46T=	ENSP00000245907.4:n.1687-46T=
ENST00000600763.1:n.320-46T=
NM_000064.3:c.1687-46T=	NP_000055.2:n.1687-46T=
NM_000064.4:c.1687-46T= MANE Select	NP_000055.2:n.1687-46T=