Canonical Allele Identifier: CA2249011272
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1906785134

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208776_14208815del , CM000679.2:g.14208776_14208815del GRCh38
NC_000017.10:g.14112093_14112132del , CM000679.1:g.14112093_14112132del GRCh37
NC_000017.9:g.14052818_14052857del NCBI36
NG_008034.1:g.144375_144414del

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*278_*281+36del
ENST00000670279.1:c.929-733_929-694del ENSP00000499450.1:n.929-733_929-694del
XR_933974.1:n.1032-733_1032-694del