Canonical Allele Identifier: CA2249011329
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208904A= , CM000679.2:g.14208904A= GRCh38
NC_000017.10:g.14112221A= , CM000679.1:g.14112221A= GRCh37
NC_000017.9:g.14052946A= NCBI36
NG_008034.1:g.144503A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+125A= ENSP00000499396.1:n.*281+125A=
ENST00000670279.1:c.929-605A= ENSP00000499450.1:n.929-605A=
XR_933974.1:n.1032-605A=