Canonical Allele Identifier: CA2636210092
Gene: COX10 HGNC NCBI

Linked Data

gnomAD v4: 17-14208774-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208774C>T , CM000679.2:g.14208774C>T GRCh38
NC_000017.10:g.14112091C>T , CM000679.1:g.14112091C>T GRCh37
NC_000017.9:g.14052816C>T NCBI36
NG_008034.1:g.144373C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*276C>T ENSP00000499396.1:n.*276C>T
ENST00000670279.1:c.929-735C>T ENSP00000499450.1:n.929-735C>T
XR_933974.1:n.1032-735C>T
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