Canonical Allele Identifier: CA439361381
Gene: RPL22P13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55087486A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000493291.1:n.194A>G
ENST00000507166.5:c.1018-53606A>G ENSP00000423325.1:n.1018-53606A>G