Canonical Allele Identifier: CA631662282
Gene: C3 HGNC NCBI

Linked Data

gnomAD v2: 19-6713782-TCCACCCCCCAGCCCCCCA-T
gnomAD v3: 19-6713771-TCCACCCCCCAGCCCCCCA-T
gnomAD v4: 19-6713771-TCCACCCCCCAGCCCCCCA-T
MyVariant Identifiers: chr19:g.6713783_6713800del (hg19) chr19:g.6713772_6713789del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713774_6713791del , CM000681.2:g.6713774_6713791del GRCh38
NC_000019.9:g.6713785_6713802del , CM000681.1:g.6713785_6713802del GRCh37
NC_000019.8:g.6664785_6664802del NCBI36
NG_009557.1:g.11863_11880del , LRG_27:g.11863_11880del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+203_650+220del ENSP00000512083.1:n.650+203_650+220del
ENST00000245907.11:c.773+203_773+220del MANE Select ENSP00000245907.4:n.773+203_773+220del
ENST00000245907.10:c.773+203_773+220del ENSP00000245907.4:n.773+203_773+220del
ENST00000595577.1:n.277+203_277+220del
NM_000064.3:c.773+203_773+220del NP_000055.2:n.773+203_773+220del
NM_000064.4:c.773+203_773+220del MANE Select NP_000055.2:n.773+203_773+220del
Search 100 bp 5'
Search 100 bp 3'