Canonical Allele Identifier: CA403642079
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6713217G>C (hg19) chr19:g.6713206G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713206G>C , CM000681.2:g.6713206G>C GRCh38
NC_000019.9:g.6713217G>C , CM000681.1:g.6713217G>C GRCh37
NC_000019.8:g.6664217G>C NCBI36
NG_009557.1:g.12446C>G , LRG_27:g.12446C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.863C>G ENSP00000512083.1:p.Thr288Ser
ENST00000695654.1:c.110C>G ENSP00000512085.1:p.Thr37Ser
ENST00000695692.1:n.310C>G
ENST00000245907.11:c.986C>G MANE Select ENSP00000245907.4:p.Thr329Ser
ENST00000245907.10:c.986C>G ENSP00000245907.4:p.Thr329Ser
ENST00000594270.5:n.110C>G
ENST00000595577.1:n.490C>G
ENST00000597442.5:n.236C>G
NM_000064.3:c.986C>G NP_000055.2:p.Thr329Ser
NM_000064.4:c.986C>G MANE Select NP_000055.2:p.Thr329Ser
Search 100 bp 5'
Search 100 bp 3'