Canonical Allele Identifier: CA498328127
Gene: COX10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.13972809T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.14069492T>A , CM000679.2:g.14069492T>A GRCh38
NC_000017.10:g.13972809T>A , CM000679.1:g.13972809T>A GRCh37
NC_000017.9:g.13913534T>A NCBI36
NG_008034.1:g.5091T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000664217.1:c.-114T>A ENSP00000499396.1:n.-114T>A
ENST00000670279.1:c.-114T>A ENSP00000499450.1:n.-114T>A
NM_001303.3:c.-114T>A NP_001294.2:n.-114T>A
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