Canonical Allele Identifier: CA726258996
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1465348526
MyVariant Identifiers: chr17:g.14112213A>C (hg19) chr17:g.14208896A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208896A>C , CM000679.2:g.14208896A>C GRCh38
NC_000017.10:g.14112213A>C , CM000679.1:g.14112213A>C GRCh37
NC_000017.9:g.14052938A>C NCBI36
NG_008034.1:g.144495A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+117A>C ENSP00000499396.1:n.*281+117A>C
ENST00000670279.1:c.929-613A>C ENSP00000499450.1:n.929-613A>C
XR_933974.1:n.1032-613A>C
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