Canonical Allele Identifier: CA2249011331
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208907C= , CM000679.2:g.14208907C= GRCh38
NC_000017.10:g.14112224C= , CM000679.1:g.14112224C= GRCh37
NC_000017.9:g.14052949C= NCBI36
NG_008034.1:g.144506C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+128C= ENSP00000499396.1:n.*281+128C=
ENST00000670279.1:c.929-602C= ENSP00000499450.1:n.929-602C=
XR_933974.1:n.1032-602C=