Canonical Allele Identifier: CA2320566128

Gene: C3

Linked Data

• dbSNP Id: rs113462415

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710051C>T , CM000681.2:g.6710051C>T	GRCh38
NC_000019.9:g.6710062C>T , CM000681.1:g.6710062C>T	GRCh37
NC_000019.8:g.6661062C>T	NCBI36
NG_009557.1:g.15601G>A , LRG_27:g.15601G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-209G>A	ENSP00000512083.1:n.1564-209G>A
ENST00000695654.1:c.811-209G>A	ENSP00000512085.1:n.811-209G>A
ENST00000695655.1:c.592-173G>A	ENSP00000512086.1:n.592-173G>A
ENST00000695692.1:n.1051-209G>A
ENST00000245907.11:c.1687-209G>A MANE Select	ENSP00000245907.4:n.1687-209G>A
ENST00000245907.10:c.1687-209G>A	ENSP00000245907.4:n.1687-209G>A
ENST00000600763.1:n.320-209G>A
NM_000064.3:c.1687-209G>A	NP_000055.2:n.1687-209G>A
NM_000064.4:c.1687-209G>A MANE Select	NP_000055.2:n.1687-209G>A