Canonical Allele Identifier: CA2587877619
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6709974-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709974A>G , CM000681.2:g.6709974A>G GRCh38
NC_000019.9:g.6709985A>G , CM000681.1:g.6709985A>G GRCh37
NC_000019.8:g.6660985A>G NCBI36
NG_009557.1:g.15678T>C , LRG_27:g.15678T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-132T>C ENSP00000512083.1:n.1564-132T>C
ENST00000695654.1:c.811-132T>C ENSP00000512085.1:n.811-132T>C
ENST00000695655.1:c.592-96T>C ENSP00000512086.1:n.592-96T>C
ENST00000695692.1:n.1051-132T>C
ENST00000245907.11:c.1687-132T>C MANE Select ENSP00000245907.4:n.1687-132T>C
ENST00000245907.10:c.1687-132T>C ENSP00000245907.4:n.1687-132T>C
ENST00000600763.1:n.320-132T>C
NM_000064.3:c.1687-132T>C NP_000055.2:n.1687-132T>C
NM_000064.4:c.1687-132T>C MANE Select NP_000055.2:n.1687-132T>C
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