Canonical Allele Identifier: CA993062085

Gene: C3

Linked Data

• dbSNP Id: rs1967573346
• gnomAD v3: 19-6697867-TCTTAGTCCACTCCGCAGGAGCTCTCCCTAACTCAG-T
• gnomAD v4: 19-6697867-TCTTAGTCCACTCCGCAGGAGCTCTCCCTAACTCAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697869_6697903del , CM000681.2:g.6697869_6697903del	GRCh38
NC_000019.9:g.6697880_6697914del , CM000681.1:g.6697880_6697914del	GRCh37
NC_000019.8:g.6648880_6648914del	NCBI36
NG_009557.1:g.27750_27784del , LRG_27:g.27750_27784del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-108_789-74del
ENST00000695652.1:c.2318-108_2318-74del	ENSP00000512083.1:n.2318-108_2318-74del
ENST00000695653.1:c.350-108_350-74del	ENSP00000512084.1:n.350-108_350-74del
ENST00000695654.1:c.1565-108_1565-74del	ENSP00000512085.1:n.1565-108_1565-74del
ENST00000695655.1:c.1382-108_1382-74del	ENSP00000512086.1:n.1382-108_1382-74del
ENST00000695692.1:n.1805-108_1805-74del
ENST00000245907.11:c.2441-108_2441-74del MANE Select	ENSP00000245907.4:n.2441-108_2441-74del
ENST00000245907.10:c.2441-108_2441-74del	ENSP00000245907.4:n.2441-108_2441-74del
ENST00000602053.1:n.489-108_489-74del
NM_000064.3:c.2441-108_2441-74del	NP_000055.2:n.2441-108_2441-74del
NM_000064.4:c.2441-108_2441-74del MANE Select	NP_000055.2:n.2441-108_2441-74del