Canonical Allele Identifier: CA2249011318
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208879A= , CM000679.2:g.14208879A= GRCh38
NC_000017.10:g.14112196A= , CM000679.1:g.14112196A= GRCh37
NC_000017.9:g.14052921A= NCBI36
NG_008034.1:g.144478A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+100A= ENSP00000499396.1:n.*281+100A=
ENST00000670279.1:c.929-630A= ENSP00000499450.1:n.929-630A=
XR_933974.1:n.1032-630A=