Canonical Allele Identifier: CA498328032
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1454729903
gnomAD v2: 17-13972798-C-G
gnomAD v3: 17-14069481-C-G
gnomAD v4: 17-14069481-C-G
MyVariant Identifiers: chr17:g.13972798C>G (hg19) chr17:g.14069481C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14069481C>G , CM000679.2:g.14069481C>G GRCh38
NC_000017.10:g.13972798C>G , CM000679.1:g.13972798C>G GRCh37
NC_000017.9:g.13913523C>G NCBI36
NG_008034.1:g.5080C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001303.3:c.-125C>G NP_001294.2:n.-125C>G
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