Canonical Allele Identifier: CA2249011330
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1906790671
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208904A>T , CM000679.2:g.14208904A>T GRCh38
NC_000017.10:g.14112221A>T , CM000679.1:g.14112221A>T GRCh37
NC_000017.9:g.14052946A>T NCBI36
NG_008034.1:g.144503A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+125A>T ENSP00000499396.1:n.*281+125A>T
ENST00000670279.1:c.929-605A>T ENSP00000499450.1:n.929-605A>T
XR_933974.1:n.1032-605A>T
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