Canonical Allele Identifier: CA498327991
Gene: COX10 HGNC NCBI

Linked Data

gnomAD v4: 17-14069475-A-G
MyVariant Identifiers: chr17:g.13972792A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14069475A>G , CM000679.2:g.14069475A>G GRCh38
NC_000017.10:g.13972792A>G , CM000679.1:g.13972792A>G GRCh37
NC_000017.9:g.13913517A>G NCBI36
NG_008034.1:g.5074A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001303.3:c.-131A>G NP_001294.2:n.-131A>G
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