Canonical Allele Identifier: CA2636210085
Gene: COX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208754A>G , CM000679.2:g.14208754A>G GRCh38
NC_000017.10:g.14112071A>G , CM000679.1:g.14112071A>G GRCh37
NC_000017.9:g.14052796A>G NCBI36
NG_008034.1:g.144353A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*256A>G ENSP00000499396.1:n.*256A>G
ENST00000670279.1:c.929-755A>G ENSP00000499450.1:n.929-755A>G
XR_933974.1:n.1032-755A>G