Canonical Allele Identifier: CA2249011328

Gene: COX10

Linked Data

• dbSNP Id: rs1906790568

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14208903T>C , CM000679.2:g.14208903T>C	GRCh38
NC_000017.10:g.14112220T>C , CM000679.1:g.14112220T>C	GRCh37
NC_000017.9:g.14052945T>C	NCBI36
NG_008034.1:g.144502T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000664217.1:c.*281+124T>C	ENSP00000499396.1:n.*281+124T>C
ENST00000670279.1:c.929-606T>C	ENSP00000499450.1:n.929-606T>C
XR_933974.1:n.1032-606T>C