Canonical Allele Identifier: CA2590736917
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs2142275089
gnomAD v3: 17-14208873-A-G
gnomAD v4: 17-14208873-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208873A>G , CM000679.2:g.14208873A>G GRCh38
NC_000017.10:g.14112190A>G , CM000679.1:g.14112190A>G GRCh37
NC_000017.9:g.14052915A>G NCBI36
NG_008034.1:g.144472A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+94A>G ENSP00000499396.1:n.*281+94A>G
ENST00000670279.1:c.929-636A>G ENSP00000499450.1:n.929-636A>G
XR_933974.1:n.1032-636A>G
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