Canonical Allele Identifier: CA498328139
Gene: COX10 HGNC NCBI

Linked Data

gnomAD v4: 17-14069494-G-C
MyVariant Identifiers: chr17:g.13972811G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14069494G>C , CM000679.2:g.14069494G>C GRCh38
NC_000017.10:g.13972811G>C , CM000679.1:g.13972811G>C GRCh37
NC_000017.9:g.13913536G>C NCBI36
NG_008034.1:g.5093G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.-112G>C ENSP00000499396.1:n.-112G>C
ENST00000670279.1:c.-112G>C ENSP00000499450.1:n.-112G>C
NM_001303.3:c.-112G>C NP_001294.2:n.-112G>C
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