Canonical Allele Identifier: CA2582310934
Gene: C3 HGNC NCBI

Linked Data

gnomAD v3: 19-6714591-GCGGCT-G
gnomAD v4: 19-6714591-GCGGCT-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714593_6714597del , CM000681.2:g.6714593_6714597del GRCh38
NC_000019.9:g.6714604_6714608del , CM000681.1:g.6714604_6714608del GRCh37
NC_000019.8:g.6665604_6665608del NCBI36
NG_009557.1:g.11056_11060del , LRG_27:g.11056_11060del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.382-150_382-146del ENSP00000512083.1:n.382-150_382-146del
ENST00000245907.11:c.505-150_505-146del MANE Select ENSP00000245907.4:n.505-150_505-146del
ENST00000245907.10:c.505-150_505-146del ENSP00000245907.4:n.505-150_505-146del
NM_000064.3:c.505-150_505-146del NP_000055.2:n.505-150_505-146del
NM_000064.4:c.505-150_505-146del MANE Select NP_000055.2:n.505-150_505-146del
Search 100 bp 5'
Search 100 bp 3'