Canonical Allele Identifier: CA2320568463

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714207G= , CM000681.2:g.6714207G=	GRCh38
NC_000019.9:g.6714218G= , CM000681.1:g.6714218G=	GRCh37
NC_000019.8:g.6665218G=	NCBI36
NG_009557.1:g.11445C= , LRG_27:g.11445C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.518C=	ENSP00000512083.1:p.Pro173=
ENST00000245907.11:c.641C= MANE Select	ENSP00000245907.4:p.Pro214=
ENST00000245907.10:c.641C=	ENSP00000245907.4:p.Pro214=
ENST00000595577.1:n.145C=
NM_000064.3:c.641C=	NP_000055.2:p.Pro214=
NM_000064.4:c.641C= MANE Select	NP_000055.2:p.Pro214=