Canonical Allele Identifier: CA691014707
Gene: RPSAP52 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65767191A>T , CM000674.2:g.65767191A>T GRCh38
NC_000012.11:g.66160971A>T , CM000674.1:g.66160971A>T GRCh37
NC_000012.10:g.64447238A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000489520.2:n.133-8160T>A
NR_026825.2:n.133-8160T>A
Search 100 bp 5'
Search 100 bp 3'