Canonical Allele Identifier: CA439361382
Gene: RPL22P13 HGNC NCBI

Linked Data

gnomAD v4: 4-54221319-A-T
MyVariant Identifiers: chr4:g.55087486A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54221319A>T , CM000666.2:g.54221319A>T GRCh38
NC_000004.11:g.55087486A>T , CM000666.1:g.55087486A>T GRCh37
NC_000004.10:g.54782243A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000493291.1:n.194A>T
ENST00000507166.5:c.1018-53606A>T ENSP00000423325.1:n.1018-53606A>T
Search 100 bp 5'
Search 100 bp 3'