Canonical Allele Identifier: CA981699424
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1906789414

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208872A>C , CM000679.2:g.14208872A>C GRCh38
NC_000017.10:g.14112189A>C , CM000679.1:g.14112189A>C GRCh37
NC_000017.9:g.14052914A>C NCBI36
NG_008034.1:g.144471A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+93A>C ENSP00000499396.1:n.*281+93A>C
ENST00000670279.1:c.929-637A>C ENSP00000499450.1:n.929-637A>C
XR_933974.1:n.1032-637A>C