Canonical Allele Identifier: CA505193133
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6713315G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713304G>C , CM000681.2:g.6713304G>C GRCh38
NC_000019.9:g.6713315G>C , CM000681.1:g.6713315G>C GRCh37
NC_000019.8:g.6664315G>C NCBI36
NG_009557.1:g.12348C>G , LRG_27:g.12348C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.765C>G ENSP00000512083.1:p.Gly255=
ENST00000695654.1:c.12C>G ENSP00000512085.1:p.Gly4=
ENST00000695692.1:n.212C>G
ENST00000245907.11:c.888C>G MANE Select ENSP00000245907.4:p.Gly296=
ENST00000245907.10:c.888C>G ENSP00000245907.4:p.Gly296=
ENST00000594270.5:n.12C>G
ENST00000595577.1:n.392C>G
ENST00000597442.5:n.138C>G
NM_000064.3:c.888C>G NP_000055.2:p.Gly296=
NM_000064.4:c.888C>G MANE Select NP_000055.2:p.Gly296=
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