Canonical Allele Identifier: CA726258943
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1193585745
MyVariant Identifiers: chr17:g.14112099G>A (hg19) chr17:g.14208782G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208782G>A , CM000679.2:g.14208782G>A GRCh38
NC_000017.10:g.14112099G>A , CM000679.1:g.14112099G>A GRCh37
NC_000017.9:g.14052824G>A NCBI36
NG_008034.1:g.144381G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+3G>A ENSP00000499396.1:n.*281+3G>A
ENST00000670279.1:c.929-727G>A ENSP00000499450.1:n.929-727G>A
XR_933974.1:n.1032-727G>A
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