Canonical Allele Identifier: CA993077892
Gene: C3 HGNC NCBI

Linked Data

gnomAD v3: 19-6713686-CA-C
gnomAD v4: 19-6713686-CA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713687del , CM000681.2:g.6713687del GRCh38
NC_000019.9:g.6713698del , CM000681.1:g.6713698del GRCh37
NC_000019.8:g.6664698del NCBI36
NG_009557.1:g.11965del , LRG_27:g.11965del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-178del ENSP00000512083.1:n.651-178del
ENST00000245907.11:c.774-178del MANE Select ENSP00000245907.4:n.774-178del
ENST00000245907.10:c.774-178del ENSP00000245907.4:n.774-178del
ENST00000595577.1:n.278-178del
ENST00000597442.5:n.23+79del
NM_000064.3:c.774-178del NP_000055.2:n.774-178del
NM_000064.4:c.774-178del MANE Select NP_000055.2:n.774-178del
Search 100 bp 5'
Search 100 bp 3'