Canonical Allele Identifier: CA2249011334
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208921C= , CM000679.2:g.14208921C= GRCh38
NC_000017.10:g.14112238C= , CM000679.1:g.14112238C= GRCh37
NC_000017.9:g.14052963C= NCBI36
NG_008034.1:g.144520C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+142C= ENSP00000499396.1:n.*281+142C=
ENST00000670279.1:c.929-588C= ENSP00000499450.1:n.929-588C=
XR_933974.1:n.1032-588C=