Canonical Allele Identifier: CA2249011286
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208797T= , CM000679.2:g.14208797T= GRCh38
NC_000017.10:g.14112114T= , CM000679.1:g.14112114T= GRCh37
NC_000017.9:g.14052839T= NCBI36
NG_008034.1:g.144396T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+18T= ENSP00000499396.1:n.*281+18T=
ENST00000670279.1:c.929-712T= ENSP00000499450.1:n.929-712T=
XR_933974.1:n.1032-712T=