Canonical Allele Identifier: CA993073483
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710016_6710037dup , CM000681.2:g.6710016_6710037dup GRCh38
NC_000019.9:g.6710027_6710048dup , CM000681.1:g.6710027_6710048dup GRCh37
NC_000019.8:g.6661027_6661048dup NCBI36
NG_009557.1:g.15626_15647dup , LRG_27:g.15626_15647dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-184_1564-163dup ENSP00000512083.1:n.1564-184_1564-163dup
ENST00000695654.1:c.811-184_811-163dup ENSP00000512085.1:n.811-184_811-163dup
ENST00000695655.1:c.592-148_592-127dup ENSP00000512086.1:n.592-148_592-127dup
ENST00000695692.1:n.1051-184_1051-163dup
ENST00000245907.11:c.1687-184_1687-163dup MANE Select ENSP00000245907.4:n.1687-184_1687-163dup
ENST00000245907.10:c.1687-184_1687-163dup ENSP00000245907.4:n.1687-184_1687-163dup
ENST00000600763.1:n.320-184_320-163dup
NM_000064.3:c.1687-184_1687-163dup NP_000055.2:n.1687-184_1687-163dup
NM_000064.4:c.1687-184_1687-163dup MANE Select NP_000055.2:n.1687-184_1687-163dup