Canonical Allele Identifier: CA505125062
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6714446G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714435G>A , CM000681.2:g.6714435G>A GRCh38
NC_000019.9:g.6714446G>A , CM000681.1:g.6714446G>A GRCh37
NC_000019.8:g.6665446G>A NCBI36
NG_009557.1:g.11217C>T , LRG_27:g.11217C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.393C>T ENSP00000512083.1:p.Gly131=
ENST00000245907.11:c.516C>T MANE Select ENSP00000245907.4:p.Gly172=
ENST00000245907.10:c.516C>T ENSP00000245907.4:p.Gly172=
NM_000064.3:c.516C>T NP_000055.2:p.Gly172=
NM_000064.4:c.516C>T MANE Select NP_000055.2:p.Gly172=
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