Canonical Allele Identifier: CA15749960

Gene: RPSAP52

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489520.2:n.133-8160T>C
NR_026825.2:n.133-8160T>C