Canonical Allele Identifier: CA2610892737
Gene: RBM20 HGNC NCBI

Linked Data

gnomAD v4: 10-110812203-CTGTG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812207_110812210del , CM000672.2:g.110812207_110812210del GRCh38
NC_000010.10:g.112571965_112571968del , CM000672.1:g.112571965_112571968del GRCh37
NC_000010.9:g.112561955_112561958del NCBI36
NG_021177.1:g.172811_172814del , LRG_382:g.172811_172814del

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.1881-71_1881-68del MANE Select ENSP00000358532.3:n.1881-71_1881-68del
ENST00000369519.3:c.1881-71_1881-68del ENSP00000358532.3:n.1881-71_1881-68del
NM_001134363.2:c.1881-71_1881-68del NP_001127835.2:n.1881-71_1881-68del
XM_011539697.1:c.1497-71_1497-68del XP_011537999.1:n.1497-71_1497-68del
XM_017016103.2:c.1716-71_1716-68del XP_016871592.1:n.1716-71_1716-68del
XM_017016104.2:c.1497-71_1497-68del XP_016871593.1:n.1497-71_1497-68del
NM_001134363.3:c.1881-71_1881-68del MANE Select NP_001127835.2:n.1881-71_1881-68del
Search 100 bp 5'
Search 100 bp 3'