Canonical Allele Identifier: CA2565677040

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709681T>C , CM000681.2:g.6709681T>C	GRCh38
NC_000019.9:g.6709692T>C , CM000681.1:g.6709692T>C	GRCh37
NC_000019.8:g.6660692T>C	NCBI36
NG_009557.1:g.15971A>G , LRG_27:g.15971A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1722+3A>G	ENSP00000512083.1:n.1722+3A>G
ENST00000695654.1:c.969+3A>G	ENSP00000512085.1:n.969+3A>G
ENST00000695655.1:c.786+3A>G	ENSP00000512086.1:n.786+3A>G
ENST00000695692.1:n.1209+3A>G
ENST00000245907.11:c.1845+3A>G MANE Select	ENSP00000245907.4:n.1845+3A>G
ENST00000245907.10:c.1845+3A>G	ENSP00000245907.4:n.1845+3A>G
NM_000064.3:c.1845+3A>G	NP_000055.2:n.1845+3A>G
NM_000064.4:c.1845+3A>G MANE Select	NP_000055.2:n.1845+3A>G