Canonical Allele Identifier: CA2249011278
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208784G= , CM000679.2:g.14208784G= GRCh38
NC_000017.10:g.14112101G= , CM000679.1:g.14112101G= GRCh37
NC_000017.9:g.14052826G= NCBI36
NG_008034.1:g.144383G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+5G= ENSP00000499396.1:n.*281+5G=
ENST00000670279.1:c.929-725G= ENSP00000499450.1:n.929-725G=
XR_933974.1:n.1032-725G=