Canonical Allele Identifier: CA439361399
Gene: RPL22P13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55087492C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54221325C>G , CM000666.2:g.54221325C>G GRCh38
NC_000004.11:g.55087492C>G , CM000666.1:g.55087492C>G GRCh37
NC_000004.10:g.54782249C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000493291.1:n.200C>G
ENST00000507166.5:c.1018-53600C>G ENSP00000423325.1:n.1018-53600C>G