Canonical Allele Identifier: CA726258947
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1264755693

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208787G>A , CM000679.2:g.14208787G>A GRCh38
NC_000017.10:g.14112104G>A , CM000679.1:g.14112104G>A GRCh37
NC_000017.9:g.14052829G>A NCBI36
NG_008034.1:g.144386G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+8G>A ENSP00000499396.1:n.*281+8G>A
ENST00000670279.1:c.929-722G>A ENSP00000499450.1:n.929-722G>A
XR_933974.1:n.1032-722G>A