Canonical Allele Identifier: CA2249011264
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1906784571

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208766A>G , CM000679.2:g.14208766A>G GRCh38
NC_000017.10:g.14112083A>G , CM000679.1:g.14112083A>G GRCh37
NC_000017.9:g.14052808A>G NCBI36
NG_008034.1:g.144365A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*268A>G ENSP00000499396.1:n.*268A>G
ENST00000670279.1:c.929-743A>G ENSP00000499450.1:n.929-743A>G
XR_933974.1:n.1032-743A>G