Canonical Allele Identifier: CA505123731

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686276A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686265A>C , CM000681.2:g.6686265A>C	GRCh38
NC_000019.9:g.6686276A>C , CM000681.1:g.6686276A>C	GRCh37
NC_000019.8:g.6637276A>C	NCBI36
NG_009557.1:g.39387T>G , LRG_27:g.39387T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2017T>G
ENST00000695652.1:c.3546T>G	ENSP00000512083.1:p.Pro1182=
ENST00000695653.1:c.1578T>G	ENSP00000512084.1:p.Pro526=
ENST00000695654.1:c.2694T>G	ENSP00000512085.1:p.Pro898=
ENST00000695655.1:c.2610T>G	ENSP00000512086.1:n.2610T>G
ENST00000695692.1:n.3033T>G
ENST00000245907.11:c.3669T>G MANE Select	ENSP00000245907.4:p.Pro1223=
ENST00000245907.10:c.3669T>G	ENSP00000245907.4:p.Pro1223=
ENST00000596238.1:n.112T>G
ENST00000601008.1:c.241+481T>G	ENSP00000471384.1:n.241+481T>G
NM_000064.3:c.3669T>G	NP_000055.2:p.Pro1223=
NM_000064.4:c.3669T>G MANE Select	NP_000055.2:p.Pro1223=