Canonical Allele Identifier: CA2587878375
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713553del , CM000681.2:g.6713553del GRCh38
NC_000019.9:g.6713564del , CM000681.1:g.6713564del GRCh37
NC_000019.8:g.6664564del NCBI36
NG_009557.1:g.12099del , LRG_27:g.12099del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-44del ENSP00000512083.1:n.651-44del
ENST00000695692.1:n.54del
ENST00000245907.11:c.774-44del MANE Select ENSP00000245907.4:n.774-44del
ENST00000245907.10:c.774-44del ENSP00000245907.4:n.774-44del
ENST00000595577.1:n.278-44del
ENST00000597442.5:n.24-44del
NM_000064.3:c.774-44del NP_000055.2:n.774-44del
NM_000064.4:c.774-44del MANE Select NP_000055.2:n.774-44del