Canonical Allele Identifier: CA993072642
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs2091058712
gnomAD v3: 19-6709501-T-TG
gnomAD v4: 19-6709501-T-TG
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709503dup , CM000681.2:g.6709503dup GRCh38
NC_000019.9:g.6709514dup , CM000681.1:g.6709514dup GRCh37
NC_000019.8:g.6660514dup NCBI36
NG_009557.1:g.16150dup , LRG_27:g.16150dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1722+182dup ENSP00000512083.1:n.1722+182dup
ENST00000695654.1:c.969+182dup ENSP00000512085.1:n.969+182dup
ENST00000695655.1:c.786+182dup ENSP00000512086.1:n.786+182dup
ENST00000695692.1:n.1209+182dup
ENST00000245907.11:c.1845+182dup MANE Select ENSP00000245907.4:n.1845+182dup
ENST00000245907.10:c.1845+182dup ENSP00000245907.4:n.1845+182dup
NM_000064.3:c.1845+182dup NP_000055.2:n.1845+182dup
NM_000064.4:c.1845+182dup MANE Select NP_000055.2:n.1845+182dup
Search 100 bp 5'
Search 100 bp 3'