Canonical Allele Identifier: CA403639137
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6709696T>C (hg19) chr19:g.6709685T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709685T>C , CM000681.2:g.6709685T>C GRCh38
NC_000019.9:g.6709696T>C , CM000681.1:g.6709696T>C GRCh37
NC_000019.8:g.6660696T>C NCBI36
NG_009557.1:g.15967A>G , LRG_27:g.15967A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.1721A>G ENSP00000512083.1:p.Lys574Arg
ENST00000695654.1:c.968A>G ENSP00000512085.1:p.Lys323Arg
ENST00000695655.1:c.785A>G ENSP00000512086.1:n.785A>G
ENST00000695692.1:n.1208A>G
ENST00000245907.11:c.1844A>G MANE Select ENSP00000245907.4:p.Lys615Arg
ENST00000245907.10:c.1844A>G ENSP00000245907.4:p.Lys615Arg
NM_000064.3:c.1844A>G NP_000055.2:p.Lys615Arg
NM_000064.4:c.1844A>G MANE Select NP_000055.2:p.Lys615Arg
Search 100 bp 5'
Search 100 bp 3'