Canonical Allele Identifier: CA2249011307
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1906788425

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208845_14208847del , CM000679.2:g.14208845_14208847del GRCh38
NC_000017.10:g.14112162_14112164del , CM000679.1:g.14112162_14112164del GRCh37
NC_000017.9:g.14052887_14052889del NCBI36
NG_008034.1:g.144444_144446del

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+66_*281+68del ENSP00000499396.1:n.*281+66_*281+68del
ENST00000670279.1:c.929-664_929-662del ENSP00000499450.1:n.929-664_929-662del
XR_933974.1:n.1032-664_1032-662del