Canonical Allele Identifier: CA439361648
Gene: RPL22P13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55087578A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54221411A>C , CM000666.2:g.54221411A>C GRCh38
NC_000004.11:g.55087578A>C , CM000666.1:g.55087578A>C GRCh37
NC_000004.10:g.54782335A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000493291.1:n.286A>C
ENST00000507166.5:c.1018-53514A>C ENSP00000423325.1:n.1018-53514A>C