Canonical Allele Identifier: CA1014970114
Gene: RPS4XP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4676371T>G , CM000682.2:g.4676371T>G GRCh38
NC_000020.10:g.4657017T>G , CM000682.1:g.4657017T>G GRCh37
NC_000020.9:g.4605017T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652447.1:n.87+8691A>C
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