Canonical Allele Identifier: CA2320558450

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6696331A= , CM000681.2:g.6696331A=	GRCh38
NC_000019.9:g.6696342A= , CM000681.1:g.6696342A=	GRCh37
NC_000019.8:g.6647342A=	NCBI36
NG_009557.1:g.29321T= , LRG_27:g.29321T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000064.4:c.2950+48T= MANE Select	NP_000055.2:n.2950+48T=
ENST00000245907.11:c.2950+48T= MANE Select	ENSP00000245907.4:n.2950+48T=
NM_000064.3:c.2950+48T=	NP_000055.2:n.2950+48T=
ENST00000245907.10:c.2950+48T=	ENSP00000245907.4:n.2950+48T=
ENST00000695651.1:n.1298+48T=
ENST00000695652.1:c.2827+48T=	ENSP00000512083.1:n.2827+48T=
ENST00000695653.1:c.859+48T=	ENSP00000512084.1:n.859+48T=
ENST00000695654.1:c.2074+48T=	ENSP00000512085.1:n.2074+48T=
ENST00000695655.1:c.1891+48T=	ENSP00000512086.1:n.1891+48T=
ENST00000695692.1:n.2314+48T=