Canonical Allele Identifier: CA403640752
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6710858T>G (hg19) chr19:g.6710847T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710847T>G , CM000681.2:g.6710847T>G GRCh38
NC_000019.9:g.6710858T>G , CM000681.1:g.6710858T>G GRCh37
NC_000019.8:g.6661858T>G NCBI36
NG_009557.1:g.14805A>C , LRG_27:g.14805A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.1357-2A>C ENSP00000512083.1:n.1357-2A>C
ENST00000695654.1:c.604-2A>C ENSP00000512085.1:n.604-2A>C
ENST00000695655.1:c.383A>C ENSP00000512086.1:p.Gln128Pro
ENST00000695692.1:n.844-2A>C
ENST00000245907.11:c.1480-2A>C MANE Select ENSP00000245907.4:n.1480-2A>C
ENST00000245907.10:c.1480-2A>C ENSP00000245907.4:n.1480-2A>C
ENST00000600763.1:n.111A>C
NM_000064.3:c.1480-2A>C NP_000055.2:n.1480-2A>C
NM_000064.4:c.1480-2A>C MANE Select NP_000055.2:n.1480-2A>C
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