Canonical Allele Identifier: CA1458520089
Gene: RPL22P13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54221322T= , CM000666.2:g.54221322T= GRCh38
NC_000004.11:g.55087489T= , CM000666.1:g.55087489T= GRCh37
NC_000004.10:g.54782246T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000493291.1:n.197T=
ENST00000507166.5:c.1018-53603T= ENSP00000423325.1:n.1018-53603T=