Canonical Allele Identifier: CA403639171
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6709705G>T (hg19) chr19:g.6709694G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709694G>T , CM000681.2:g.6709694G>T GRCh38
NC_000019.9:g.6709705G>T , CM000681.1:g.6709705G>T GRCh37
NC_000019.8:g.6660705G>T NCBI36
NG_009557.1:g.15958C>A , LRG_27:g.15958C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1712C>A ENSP00000512083.1:p.Thr571Lys
ENST00000695654.1:c.959C>A ENSP00000512085.1:p.Thr320Lys
ENST00000695655.1:c.776C>A ENSP00000512086.1:n.776C>A
ENST00000695692.1:n.1199C>A
ENST00000245907.11:c.1835C>A MANE Select ENSP00000245907.4:p.Thr612Lys
ENST00000245907.10:c.1835C>A ENSP00000245907.4:p.Thr612Lys
NM_000064.3:c.1835C>A NP_000055.2:p.Thr612Lys
NM_000064.4:c.1835C>A MANE Select NP_000055.2:p.Thr612Lys
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