Canonical Allele Identifier: CA884131648
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1204084236
gnomAD v3: 19-6713663-AG-A
gnomAD v4: 19-6713663-AG-A
MyVariant Identifiers: chr19:g.6713675del (hg19) chr19:g.6713664del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713664del , CM000681.2:g.6713664del GRCh38
NC_000019.9:g.6713675del , CM000681.1:g.6713675del GRCh37
NC_000019.8:g.6664675del NCBI36
NG_009557.1:g.11988del , LRG_27:g.11988del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-155del ENSP00000512083.1:n.651-155del
ENST00000245907.11:c.774-155del MANE Select ENSP00000245907.4:n.774-155del
ENST00000245907.10:c.774-155del ENSP00000245907.4:n.774-155del
ENST00000595577.1:n.278-155del
ENST00000597442.5:n.23+102del
NM_000064.3:c.774-155del NP_000055.2:n.774-155del
NM_000064.4:c.774-155del MANE Select NP_000055.2:n.774-155del
Search 100 bp 5'
Search 100 bp 3'