Canonical Allele Identifier: CA2587877515
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6709862-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709862G>T , CM000681.2:g.6709862G>T GRCh38
NC_000019.9:g.6709873G>T , CM000681.1:g.6709873G>T GRCh37
NC_000019.8:g.6660873G>T NCBI36
NG_009557.1:g.15790C>A , LRG_27:g.15790C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-20C>A ENSP00000512083.1:n.1564-20C>A
ENST00000695654.1:c.811-20C>A ENSP00000512085.1:n.811-20C>A
ENST00000695655.1:c.608C>A ENSP00000512086.1:n.608C>A
ENST00000695692.1:n.1051-20C>A
ENST00000245907.11:c.1687-20C>A MANE Select ENSP00000245907.4:n.1687-20C>A
ENST00000245907.10:c.1687-20C>A ENSP00000245907.4:n.1687-20C>A
ENST00000600763.1:n.320-20C>A
NM_000064.3:c.1687-20C>A NP_000055.2:n.1687-20C>A
NM_000064.4:c.1687-20C>A MANE Select NP_000055.2:n.1687-20C>A
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