Canonical Allele Identifier: CA726258942
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1425540970
MyVariant Identifiers: chr17:g.14112084G>T (hg19) chr17:g.14208767G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208767G>T , CM000679.2:g.14208767G>T GRCh38
NC_000017.10:g.14112084G>T , CM000679.1:g.14112084G>T GRCh37
NC_000017.9:g.14052809G>T NCBI36
NG_008034.1:g.144366G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*269G>T ENSP00000499396.1:n.*269G>T
ENST00000670279.1:c.929-742G>T ENSP00000499450.1:n.929-742G>T
XR_933974.1:n.1032-742G>T
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