Canonical Allele Identifier: CA439361576
Gene: RPL22P13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55087553G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54221386G>C , CM000666.2:g.54221386G>C GRCh38
NC_000004.11:g.55087553G>C , CM000666.1:g.55087553G>C GRCh37
NC_000004.10:g.54782310G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000493291.1:n.261G>C
ENST00000507166.5:c.1018-53539G>C ENSP00000423325.1:n.1018-53539G>C