Canonical Allele Identifier: CA2249011248
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208737G= , CM000679.2:g.14208737G= GRCh38
NC_000017.10:g.14112054G= , CM000679.1:g.14112054G= GRCh37
NC_000017.9:g.14052779G= NCBI36
NG_008034.1:g.144336G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*239G= ENSP00000499396.1:n.*239G=
ENST00000670279.1:c.929-772G= ENSP00000499450.1:n.929-772G=
XR_933974.1:n.1032-772G=