Canonical Allele Identifier: CA914295426
Gene: C3 HGNC NCBI

Linked Data

gnomAD v2: 19-6713672-CCAG-C
gnomAD v3: 19-6713661-CCAG-C
gnomAD v4: 19-6713661-CCAG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713663_6713665del , CM000681.2:g.6713663_6713665del GRCh38
NC_000019.9:g.6713674_6713676del , CM000681.1:g.6713674_6713676del GRCh37
NC_000019.8:g.6664674_6664676del NCBI36
NG_009557.1:g.11988_11990del , LRG_27:g.11988_11990del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-155_651-153del ENSP00000512083.1:n.651-155_651-153del
ENST00000245907.11:c.774-155_774-153del MANE Select ENSP00000245907.4:n.774-155_774-153del
ENST00000245907.10:c.774-155_774-153del ENSP00000245907.4:n.774-155_774-153del
ENST00000595577.1:n.278-155_278-153del
ENST00000597442.5:n.23+102_23+104del
NM_000064.3:c.774-155_774-153del NP_000055.2:n.774-155_774-153del
NM_000064.4:c.774-155_774-153del MANE Select NP_000055.2:n.774-155_774-153del
Search 100 bp 5'
Search 100 bp 3'