Canonical Allele Identifier: CA2320555676

Gene: C3

Linked Data

• dbSNP Id: rs565370206

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6690503T>A , CM000681.2:g.6690503T>A	GRCh38
NC_000019.9:g.6690514T>A , CM000681.1:g.6690514T>A	GRCh37
NC_000019.8:g.6641514T>A	NCBI36
NG_009557.1:g.35149A>T , LRG_27:g.35149A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.1837+126A>T
ENST00000695652.1:c.3366+126A>T	ENSP00000512083.1:n.3366+126A>T
ENST00000695653.1:c.1398+126A>T	ENSP00000512084.1:n.1398+126A>T
ENST00000695654.1:c.2514+2421A>T	ENSP00000512085.1:n.2514+2421A>T
ENST00000695655.1:c.2430+126A>T	ENSP00000512086.1:n.2430+126A>T
ENST00000695692.1:n.2853+126A>T
ENST00000245907.11:c.3489+126A>T MANE Select	ENSP00000245907.4:n.3489+126A>T
ENST00000245907.10:c.3489+126A>T	ENSP00000245907.4:n.3489+126A>T
ENST00000598805.2:n.259+126A>T
ENST00000601008.1:c.84+126A>T	ENSP00000471384.1:n.84+126A>T
NM_000064.3:c.3489+126A>T	NP_000055.2:n.3489+126A>T
NM_000064.4:c.3489+126A>T MANE Select	NP_000055.2:n.3489+126A>T