Canonical Allele Identifier: CA439361391

Gene: RPL22P13

Linked Data

• dbSNP Id: rs1720288925
• MyVariant Identifiers: chr4:g.55087489T>G (hg19)

Genomic Alleles

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

Transcript Alleles

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