Canonical Allele Identifier: CA884128350

Gene: C3

Linked Data

• dbSNP Id: rs1373091840
• MyVariant Identifiers: chr19:g.6679378_6679382del (hg19) ; chr19:g.6679367_6679371del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679367_6679371del , CM000681.2:g.6679367_6679371del	GRCh38
NC_000019.9:g.6679378_6679382del , CM000681.1:g.6679378_6679382del	GRCh37
NC_000019.8:g.6630378_6630382del	NCBI36
NG_009557.1:g.46281_46285del , LRG_27:g.46281_46285del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2894+36_2894+40del
ENST00000695653.1:c.2455+36_2455+40del	ENSP00000512084.1:n.2455+36_2455+40del
ENST00000695654.1:c.3571+36_3571+40del	ENSP00000512085.1:n.3571+36_3571+40del
ENST00000695689.1:c.517+36_517+40del	ENSP00000512101.1:n.517+36_517+40del
ENST00000695690.1:n.1611+36_1611+40del
ENST00000695691.1:n.1407+36_1407+40del
ENST00000245907.11:c.4546+36_4546+40del MANE Select	ENSP00000245907.4:n.4546+36_4546+40del
ENST00000245907.10:c.4546+36_4546+40del	ENSP00000245907.4:n.4546+36_4546+40del
ENST00000599668.1:n.166+11_166+15del
ENST00000599899.5:n.1505+36_1505+40del
ENST00000601008.1:c.242-1413_242-1409del	ENSP00000471384.1:n.242-1413_242-1409del
NM_000064.3:c.4546+36_4546+40del	NP_000055.2:n.4546+36_4546+40del
NM_000064.4:c.4546+36_4546+40del MANE Select	NP_000055.2:n.4546+36_4546+40del