Canonical Allele Identifier: CA2582310935
Gene: C3 HGNC NCBI

Linked Data

gnomAD v3: 19-6714598-ACG-A
gnomAD v4: 19-6714598-ACG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714600_6714601del , CM000681.2:g.6714600_6714601del GRCh38
NC_000019.9:g.6714611_6714612del , CM000681.1:g.6714611_6714612del GRCh37
NC_000019.8:g.6665611_6665612del NCBI36
NG_009557.1:g.11052_11053del , LRG_27:g.11052_11053del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.382-154_382-153del ENSP00000512083.1:n.382-154_382-153del
ENST00000245907.11:c.505-154_505-153del MANE Select ENSP00000245907.4:n.505-154_505-153del
ENST00000245907.10:c.505-154_505-153del ENSP00000245907.4:n.505-154_505-153del
NM_000064.3:c.505-154_505-153del NP_000055.2:n.505-154_505-153del
NM_000064.4:c.505-154_505-153del MANE Select NP_000055.2:n.505-154_505-153del
Search 100 bp 5'
Search 100 bp 3'