Canonical Allele Identifier: CA2320559271

Gene: C3

Linked Data

• dbSNP Id: rs1967573384
• gnomAD v4: 19-6697868-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697869_6697870del , CM000681.2:g.6697869_6697870del	GRCh38
NC_000019.9:g.6697880_6697881del , CM000681.1:g.6697880_6697881del	GRCh37
NC_000019.8:g.6648880_6648881del	NCBI36
NG_009557.1:g.27782_27783del , LRG_27:g.27782_27783del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-76_789-75del
ENST00000695652.1:c.2318-76_2318-75del	ENSP00000512083.1:n.2318-76_2318-75del
ENST00000695653.1:c.350-76_350-75del	ENSP00000512084.1:n.350-76_350-75del
ENST00000695654.1:c.1565-76_1565-75del	ENSP00000512085.1:n.1565-76_1565-75del
ENST00000695655.1:c.1382-76_1382-75del	ENSP00000512086.1:n.1382-76_1382-75del
ENST00000695692.1:n.1805-76_1805-75del
ENST00000245907.11:c.2441-76_2441-75del MANE Select	ENSP00000245907.4:n.2441-76_2441-75del
ENST00000245907.10:c.2441-76_2441-75del	ENSP00000245907.4:n.2441-76_2441-75del
ENST00000602053.1:n.489-76_489-75del
NM_000064.3:c.2441-76_2441-75del	NP_000055.2:n.2441-76_2441-75del
NM_000064.4:c.2441-76_2441-75del MANE Select	NP_000055.2:n.2441-76_2441-75del