Canonical Allele Identifier: CA505193111
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6713460G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713449G>C , CM000681.2:g.6713449G>C GRCh38
NC_000019.9:g.6713460G>C , CM000681.1:g.6713460G>C GRCh37
NC_000019.8:g.6664460G>C NCBI36
NG_009557.1:g.12203C>G , LRG_27:g.12203C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.711C>G ENSP00000512083.1:p.Gly237=
ENST00000695692.1:n.158C>G
ENST00000245907.11:c.834C>G MANE Select ENSP00000245907.4:p.Gly278=
ENST00000245907.10:c.834C>G ENSP00000245907.4:p.Gly278=
ENST00000595577.1:n.338C>G
ENST00000597442.5:n.84C>G
NM_000064.3:c.834C>G NP_000055.2:p.Gly278=
NM_000064.4:c.834C>G MANE Select NP_000055.2:p.Gly278=
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