Canonical Allele Identifier: CA2249011256
Gene: COX10 HGNC NCBI

Linked Data

dbSNP Id: rs1906783617

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14208753G>C , CM000679.2:g.14208753G>C GRCh38
NC_000017.10:g.14112070G>C , CM000679.1:g.14112070G>C GRCh37
NC_000017.9:g.14052795G>C NCBI36
NG_008034.1:g.144352G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.*255G>C ENSP00000499396.1:n.*255G>C
ENST00000670279.1:c.929-756G>C ENSP00000499450.1:n.929-756G>C
XR_933974.1:n.1032-756G>C