Canonical Allele Identifier: CA288082299
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs748869777

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208805G>A , CM000679.2:g.14208805G>A GRCh38
NC_000017.10:g.14112122G>A , CM000679.1:g.14112122G>A GRCh37
NC_000017.9:g.14052847G>A NCBI36
NG_008034.1:g.144404G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+26G>A ENSP00000499396.1:n.*281+26G>A
ENST00000670279.1:c.929-704G>A ENSP00000499450.1:n.929-704G>A
XR_933974.1:n.1032-704G>A