Canonical Allele Identifier: CA505192998
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6713222A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713211A>C , CM000681.2:g.6713211A>C GRCh38
NC_000019.9:g.6713222A>C , CM000681.1:g.6713222A>C GRCh37
NC_000019.8:g.6664222A>C NCBI36
NG_009557.1:g.12441T>G , LRG_27:g.12441T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.858T>G ENSP00000512083.1:p.Ser286=
ENST00000695654.1:c.105T>G ENSP00000512085.1:p.Ser35=
ENST00000695692.1:n.305T>G
ENST00000245907.11:c.981T>G MANE Select ENSP00000245907.4:p.Ser327=
ENST00000245907.10:c.981T>G ENSP00000245907.4:p.Ser327=
ENST00000594270.5:n.105T>G
ENST00000595577.1:n.485T>G
ENST00000597442.5:n.231T>G
NM_000064.3:c.981T>G NP_000055.2:p.Ser327=
NM_000064.4:c.981T>G MANE Select NP_000055.2:p.Ser327=
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