Canonical Allele Identifier: CA2249011312
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs143094081
gnomAD v3: 17-14208857-A-G
gnomAD v4: 17-14208857-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208857A>G , CM000679.2:g.14208857A>G GRCh38
NC_000017.10:g.14112174A>G , CM000679.1:g.14112174A>G GRCh37
NC_000017.9:g.14052899A>G NCBI36
NG_008034.1:g.144456A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*281+78A>G ENSP00000499396.1:n.*281+78A>G
ENST00000670279.1:c.929-652A>G ENSP00000499450.1:n.929-652A>G
XR_933974.1:n.1032-652A>G
Search 100 bp 5'
Search 100 bp 3'