Canonical Allele Identifier: CA439361392

Gene: RPL22P13

Linked Data

• dbSNP Id: rs1720288961
• gnomAD v4: 4-54221323-C-A
• MyVariant Identifiers: chr4:g.55087490C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54221323C>A , CM000666.2:g.54221323C>A	GRCh38
NC_000004.11:g.55087490C>A , CM000666.1:g.55087490C>A	GRCh37
NC_000004.10:g.54782247C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000493291.1:n.198C>A
ENST00000507166.5:c.1018-53602C>A	ENSP00000423325.1:n.1018-53602C>A