Canonical Allele Identifier: CA631662291
Gene: C3 HGNC NCBI

Linked Data

gnomAD v2: 19-6713803-TGGTCCCACCCCCAGCC-T
gnomAD v3: 19-6713792-TGGTCCCACCCCCAGCC-T
gnomAD v4: 19-6713792-TGGTCCCACCCCCAGCC-T
MyVariant Identifiers: chr19:g.6713804_6713819del (hg19) chr19:g.6713793_6713808del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713793_6713808del , CM000681.2:g.6713793_6713808del GRCh38
NC_000019.9:g.6713804_6713819del , CM000681.1:g.6713804_6713819del GRCh37
NC_000019.8:g.6664804_6664819del NCBI36
NG_009557.1:g.11844_11859del , LRG_27:g.11844_11859del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+184_650+199del ENSP00000512083.1:n.650+184_650+199del
ENST00000245907.11:c.773+184_773+199del MANE Select ENSP00000245907.4:n.773+184_773+199del
ENST00000245907.10:c.773+184_773+199del ENSP00000245907.4:n.773+184_773+199del
ENST00000595577.1:n.277+184_277+199del
NM_000064.3:c.773+184_773+199del NP_000055.2:n.773+184_773+199del
NM_000064.4:c.773+184_773+199del MANE Select NP_000055.2:n.773+184_773+199del
Search 100 bp 5'
Search 100 bp 3'