Canonical Allele Identifier: CA624926453
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1180071908
gnomAD v2: 17-14112212-G-A
gnomAD v3: 17-14208895-G-A
gnomAD v4: 17-14208895-G-A
MyVariant Identifiers: chr17:g.14112212G>A (hg19) chr17:g.14208895G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208895G>A , CM000679.2:g.14208895G>A GRCh38
NC_000017.10:g.14112212G>A , CM000679.1:g.14112212G>A GRCh37
NC_000017.9:g.14052937G>A NCBI36
NG_008034.1:g.144494G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+116G>A ENSP00000499396.1:n.*281+116G>A
ENST00000670279.1:c.929-614G>A ENSP00000499450.1:n.929-614G>A
XR_933974.1:n.1032-614G>A
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