Canonical Allele Identifier: CA2249011251
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208746G= , CM000679.2:g.14208746G= GRCh38
NC_000017.10:g.14112063G= , CM000679.1:g.14112063G= GRCh37
NC_000017.9:g.14052788G= NCBI36
NG_008034.1:g.144345G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*248G= ENSP00000499396.1:n.*248G=
ENST00000670279.1:c.929-763G= ENSP00000499450.1:n.929-763G=
XR_933974.1:n.1032-763G=