Canonical Allele Identifier: CA439361343

Gene: RPL22P13

Linked Data

• dbSNP Id: rs1027333348
• gnomAD v4: 4-54221306-C-A
• MyVariant Identifiers: chr4:g.55087473C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54221306C>A , CM000666.2:g.54221306C>A	GRCh38
NC_000004.11:g.55087473C>A , CM000666.1:g.55087473C>A	GRCh37
NC_000004.10:g.54782230C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493291.1:n.181C>A
ENST00000507166.5:c.1018-53619C>A	ENSP00000423325.1:n.1018-53619C>A