Canonical Allele Identifier: CA993077834
Gene: C3 HGNC NCBI

Linked Data

gnomAD v3: 19-6713654-C-CCT
gnomAD v4: 19-6713654-C-CCT
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713655_6713656insTC , CM000681.2:g.6713655_6713656insTC GRCh38
NC_000019.9:g.6713666_6713667insTC , CM000681.1:g.6713666_6713667insTC GRCh37
NC_000019.8:g.6664666_6664667insTC NCBI36
NG_009557.1:g.11997_11998insAG , LRG_27:g.11997_11998insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-146_651-145insAG ENSP00000512083.1:n.651-146_651-145insAG
ENST00000245907.11:c.774-146_774-145insAG MANE Select ENSP00000245907.4:n.774-146_774-145insAG
ENST00000245907.10:c.774-146_774-145insAG ENSP00000245907.4:n.774-146_774-145insAG
ENST00000595577.1:n.278-146_278-145insAG
ENST00000597442.5:n.23+111_23+112insAG
NM_000064.3:c.774-146_774-145insAG NP_000055.2:n.774-146_774-145insAG
NM_000064.4:c.774-146_774-145insAG MANE Select NP_000055.2:n.774-146_774-145insAG
Search 100 bp 5'
Search 100 bp 3'