Canonical Allele Identifier: CA498327934
Gene: COX10 HGNC NCBI

Linked Data

gnomAD v4: 17-14069468-C-T
MyVariant Identifiers: chr17:g.13972785C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14069468C>T , CM000679.2:g.14069468C>T GRCh38
NC_000017.10:g.13972785C>T , CM000679.1:g.13972785C>T GRCh37
NC_000017.9:g.13913510C>T NCBI36
NG_008034.1:g.5067C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001303.3:c.-138C>T NP_001294.2:n.-138C>T
Search 100 bp 5'
Search 100 bp 3'