Canonical Allele Identifier: CA2249011322
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1906790080

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208882A>G , CM000679.2:g.14208882A>G GRCh38
NC_000017.10:g.14112199A>G , CM000679.1:g.14112199A>G GRCh37
NC_000017.9:g.14052924A>G NCBI36
NG_008034.1:g.144481A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+103A>G ENSP00000499396.1:n.*281+103A>G
ENST00000670279.1:c.929-627A>G ENSP00000499450.1:n.929-627A>G
XR_933974.1:n.1032-627A>G