Canonical Allele Identifier: CA439361390

Gene: RPL22P13

Linked Data

• gnomAD v4: 4-54221322-T-C
• MyVariant Identifiers: chr4:g.55087489T>C (hg19)

Genomic Alleles

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

Transcript Alleles

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