Canonical Allele Identifier: CA2733000142
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs2142274845
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208565G>C , CM000679.2:g.14208565G>C GRCh38
NC_000017.10:g.14111882G>C , CM000679.1:g.14111882G>C GRCh37
NC_000017.9:g.14052607G>C NCBI36
NG_008034.1:g.144164G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261643.8:c.*1352G>C MANE Select ENSP00000261643.3:n.*1352G>C
ENST00000664217.1:c.*67G>C ENSP00000499396.1:n.*67G>C
ENST00000670279.1:c.929-944G>C ENSP00000499450.1:n.929-944G>C
ENST00000261643.7:c.*1352G>C ENSP00000261643.3:n.*1352G>C
NM_001303.3:c.*1352G>C NP_001294.2:n.*1352G>C
XM_011523658.1:c.*1352G>C XP_011521960.1:n.*1352G>C
XR_933974.1:n.1032-944G>C
NM_001303.4:c.*1352G>C MANE Select NP_001294.2:n.*1352G>C
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