Canonical Allele Identifier: CA439361379
Gene: RPL22P13 HGNC NCBI

Linked Data

dbSNP Id: rs1389222401
gnomAD v3: 4-54221318-C-T
gnomAD v4: 4-54221318-C-T
MyVariant Identifiers: chr4:g.55087485C>T (hg19) chr4:g.54221318C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54221318C>T , CM000666.2:g.54221318C>T GRCh38
NC_000004.11:g.55087485C>T , CM000666.1:g.55087485C>T GRCh37
NC_000004.10:g.54782242C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000493291.1:n.193C>T
ENST00000507166.5:c.1018-53607C>T ENSP00000423325.1:n.1018-53607C>T
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