Canonical Allele Identifier: CA2636210087
Gene: COX10 HGNC NCBI

Linked Data

gnomAD v4: 17-14208759-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208759G>T , CM000679.2:g.14208759G>T GRCh38
NC_000017.10:g.14112076G>T , CM000679.1:g.14112076G>T GRCh37
NC_000017.9:g.14052801G>T NCBI36
NG_008034.1:g.144358G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*261G>T ENSP00000499396.1:n.*261G>T
ENST00000670279.1:c.929-750G>T ENSP00000499450.1:n.929-750G>T
XR_933974.1:n.1032-750G>T
Search 100 bp 5'
Search 100 bp 3'