Canonical Allele Identifier: CA498328034
Gene: COX10 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
NM_001303.3:c.-125C>T NP_001294.2:n.-125C>T
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Search 100 bp 3'