Canonical Allele Identifier: CA2636210143
Gene: COX10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208792T>C , CM000679.2:g.14208792T>C GRCh38
NC_000017.10:g.14112109T>C , CM000679.1:g.14112109T>C GRCh37
NC_000017.9:g.14052834T>C NCBI36
NG_008034.1:g.144391T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+13T>C ENSP00000499396.1:n.*281+13T>C
ENST00000670279.1:c.929-717T>C ENSP00000499450.1:n.929-717T>C
XR_933974.1:n.1032-717T>C