Canonical Allele Identifier: CA1458520144
Gene: RPL22P13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54221396G= , CM000666.2:g.54221396G= GRCh38
NC_000004.11:g.55087563G= , CM000666.1:g.55087563G= GRCh37
NC_000004.10:g.54782320G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000493291.1:n.271G=
ENST00000507166.5:c.1018-53529G= ENSP00000423325.1:n.1018-53529G=