Canonical Allele Identifier: CA439361402
Gene: RPL22P13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55087493T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54221326T>C , CM000666.2:g.54221326T>C GRCh38
NC_000004.11:g.55087493T>C , CM000666.1:g.55087493T>C GRCh37
NC_000004.10:g.54782250T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000493291.1:n.201T>C
ENST00000507166.5:c.1018-53599T>C ENSP00000423325.1:n.1018-53599T>C