Canonical Allele Identifier: CA1458520159
Gene: RPL22P13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54221414C= , CM000666.2:g.54221414C= GRCh38
NC_000004.11:g.55087581C= , CM000666.1:g.55087581C= GRCh37
NC_000004.10:g.54782338C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000493291.1:n.289C=
ENST00000507166.5:c.1018-53511C= ENSP00000423325.1:n.1018-53511C=