Canonical Allele Identifier: CA993078307
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs774491432
gnomAD v3: 19-6714288-G-GC
gnomAD v4: 19-6714288-G-GC
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714294dup , CM000681.2:g.6714294dup GRCh38
NC_000019.9:g.6714305dup , CM000681.1:g.6714305dup GRCh37
NC_000019.8:g.6665305dup NCBI36
NG_009557.1:g.11363dup , LRG_27:g.11363dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.477-41dup ENSP00000512083.1:n.477-41dup
ENST00000245907.11:c.600-41dup MANE Select ENSP00000245907.4:n.600-41dup
ENST00000245907.10:c.600-41dup ENSP00000245907.4:n.600-41dup
ENST00000595577.1:n.63dup
NM_000064.3:c.600-41dup NP_000055.2:n.600-41dup
NM_000064.4:c.600-41dup MANE Select NP_000055.2:n.600-41dup
Search 100 bp 5'
Search 100 bp 3'