Canonical Allele Identifier: CA2248956543
Gene: COX10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14069491G= , CM000679.2:g.14069491G= GRCh38
NC_000017.10:g.13972808G= , CM000679.1:g.13972808G= GRCh37
NC_000017.9:g.13913533G= NCBI36
NG_008034.1:g.5090G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.-115G= ENSP00000499396.1:n.-115G=
ENST00000670279.1:c.-115G= ENSP00000499450.1:n.-115G=
NM_001303.3:c.-115G= NP_001294.2:n.-115G=