Canonical Allele Identifier: CA2320567952

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713507A= , CM000681.2:g.6713507A=	GRCh38
NC_000019.9:g.6713518A= , CM000681.1:g.6713518A=	GRCh37
NC_000019.8:g.6664518A=	NCBI36
NG_009557.1:g.12145T= , LRG_27:g.12145T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.653T=	ENSP00000512083.1:p.Phe218=
ENST00000695692.1:n.100T=
ENST00000245907.11:c.776T= MANE Select	ENSP00000245907.4:p.Phe259=
ENST00000245907.10:c.776T=	ENSP00000245907.4:p.Phe259=
ENST00000595577.1:n.280T=
ENST00000597442.5:n.26T=
NM_000064.3:c.776T=	NP_000055.2:p.Phe259=
NM_000064.4:c.776T= MANE Select	NP_000055.2:p.Phe259=