Canonical Allele Identifier: CA439361389
Gene: RPL22P13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55087489T>A (hg19)
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Genomic Alleles

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

Transcript Alleles

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