Canonical Allele Identifier: CA918760099
Gene: RBM20 HGNC NCBI

Linked Data

dbSNP Id: rs1590591070
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110644604_110644609dup , CM000672.2:g.110644604_110644609dup GRCh38
NC_000010.10:g.112404362_112404367dup , CM000672.1:g.112404362_112404367dup GRCh37
NC_000010.9:g.112394352_112394357dup NCBI36
NG_021177.1:g.5208_5213dup , LRG_382:g.5208_5213dup

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.150_155dup MANE Select ENSP00000358532.3:p.Pro52_Pro53insProPro
ENST00000369519.3:c.150_155dup ENSP00000358532.3:p.Pro52_Pro53insProPro
NM_001134363.2:c.150_155dup NP_001127835.2:p.Pro52_Pro53insProPro
XM_017016103.2:c.26+1164_26+1169dup XP_016871592.1:n.26+1164_26+1169dup
NM_001134363.3:c.150_155dup MANE Select NP_001127835.2:p.Pro52_Pro53insProPro
Search 100 bp 5'
Search 100 bp 3'