Canonical Allele Identifier: CA884129426
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1163281743
MyVariant Identifiers: chr19:g.6710869G>T (hg19) chr19:g.6710858G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710858G>T , CM000681.2:g.6710858G>T GRCh38
NC_000019.9:g.6710869G>T , CM000681.1:g.6710869G>T GRCh37
NC_000019.8:g.6661869G>T NCBI36
NG_009557.1:g.14794C>A , LRG_27:g.14794C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1357-13C>A ENSP00000512083.1:n.1357-13C>A
ENST00000695654.1:c.604-13C>A ENSP00000512085.1:n.604-13C>A
ENST00000695655.1:c.372C>A ENSP00000512086.1:p.Ser124Arg
ENST00000695692.1:n.844-13C>A
ENST00000245907.11:c.1480-13C>A MANE Select ENSP00000245907.4:n.1480-13C>A
ENST00000245907.10:c.1480-13C>A ENSP00000245907.4:n.1480-13C>A
ENST00000600763.1:n.100C>A
NM_000064.3:c.1480-13C>A NP_000055.2:n.1480-13C>A
NM_000064.4:c.1480-13C>A MANE Select NP_000055.2:n.1480-13C>A
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