Canonical Allele Identifier: CA498328054
Gene: COX10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.13972800C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14069483C>G , CM000679.2:g.14069483C>G GRCh38
NC_000017.10:g.13972800C>G , CM000679.1:g.13972800C>G GRCh37
NC_000017.9:g.13913525C>G NCBI36
NG_008034.1:g.5082C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001303.3:c.-123C>G NP_001294.2:n.-123C>G
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