ClinGen Allele Registry
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Canonical Allele Identifier:
CA744879952
Gene: RPS4XP2
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.4675114C>G , CM000682.2:g.4675114C>G
GRCh38
NC_000020.10:g.4655760C>G , CM000682.1:g.4655760C>G
GRCh37
NC_000020.9:g.4603760C>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000652447.1:n.87+9948G>C
Search 100 bp 5'
Search 100 bp 3'