Canonical Allele Identifier: CA439361378

Gene: RPL22P13

Linked Data

• dbSNP Id: rs1389222401
• MyVariant Identifiers: chr4:g.55087485C>G (hg19)

Genomic Alleles

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

Transcript Alleles

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