Canonical Allele Identifier: CA726258982

Gene: COX10

Linked Data

• dbSNP Id: rs1443253739
• MyVariant Identifiers: chr17:g.14112147A>G (hg19) ; chr17:g.14208830A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14208830A>G , CM000679.2:g.14208830A>G	GRCh38
NC_000017.10:g.14112147A>G , CM000679.1:g.14112147A>G	GRCh37
NC_000017.9:g.14052872A>G	NCBI36
NG_008034.1:g.144429A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000664217.1:c.*281+51A>G	ENSP00000499396.1:n.*281+51A>G
ENST00000670279.1:c.929-679A>G	ENSP00000499450.1:n.929-679A>G
XR_933974.1:n.1032-679A>G