Canonical Allele Identifier: CA2320567743

Gene: C3

Linked Data

• dbSNP Id: rs974416047

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713004C>A , CM000681.2:g.6713004C>A	GRCh38
NC_000019.9:g.6713015C>A , CM000681.1:g.6713015C>A	GRCh37
NC_000019.8:g.6664015C>A	NCBI36
NG_009557.1:g.12648G>T , LRG_27:g.12648G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.880+185G>T	ENSP00000512083.1:n.880+185G>T
ENST00000695654.1:c.127+185G>T	ENSP00000512085.1:n.127+185G>T
ENST00000695692.1:n.327+185G>T
ENST00000245907.11:c.1003+185G>T MANE Select	ENSP00000245907.4:n.1003+185G>T
ENST00000245907.10:c.1003+185G>T	ENSP00000245907.4:n.1003+185G>T
ENST00000594270.5:n.127+185G>T
ENST00000595577.1:n.507+185G>T
ENST00000597442.5:n.253+185G>T
NM_000064.3:c.1003+185G>T	NP_000055.2:n.1003+185G>T
NM_000064.4:c.1003+185G>T MANE Select	NP_000055.2:n.1003+185G>T