Canonical Allele Identifier: CA439361365

Gene: RPL22P13

Linked Data

• dbSNP Id: rs1720288788
• MyVariant Identifiers: chr4:g.55087481G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54221314G>A , CM000666.2:g.54221314G>A	GRCh38
NC_000004.11:g.55087481G>A , CM000666.1:g.55087481G>A	GRCh37
NC_000004.10:g.54782238G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000493291.1:n.189G>A
ENST00000507166.5:c.1018-53611G>A	ENSP00000423325.1:n.1018-53611G>A