Canonical Allele Identifier: CA403629837

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6694620G>A , CM000681.2:g.6694620G>A	GRCh38
NC_000019.9:g.6694631G>A , CM000681.1:g.6694631G>A	GRCh37
NC_000019.8:g.6645631G>A	NCBI36
NG_009557.1:g.31032C>T , LRG_27:g.31032C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000064.4:c.2965C>T MANE Select	NP_000055.2:p.Gln989Ter
ENST00000245907.11:c.2965C>T MANE Select	ENSP00000245907.4:p.Gln989Ter
NM_000064.3:c.2965C>T	NP_000055.2:p.Gln989Ter
ENST00000245907.10:c.2965C>T	ENSP00000245907.4:p.Gln989Ter
ENST00000695651.1:n.1313C>T
ENST00000695652.1:c.2842C>T	ENSP00000512083.1:p.Gln948Ter
ENST00000695653.1:c.874C>T	ENSP00000512084.1:p.Gln292Ter
ENST00000695654.1:c.2089C>T	ENSP00000512085.1:p.Gln697Ter
ENST00000695655.1:c.1906C>T	ENSP00000512086.1:n.1906C>T
ENST00000695692.1:n.2329C>T