Canonical Allele Identifier: CA2347150322
Community Standard Title: NC_000020.11:g.4684616A=
Gene: RPS4XP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4684616A= , CM000682.2:g.4684616A= GRCh38
NC_000020.10:g.4665262A= , CM000682.1:g.4665262A= GRCh37
NC_000020.9:g.4613262A= NCBI36
NG_009087.1:g.3466A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000652447.1:n.87+446T=