Canonical Allele Identifier: CA378380437
Gene: RBM20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110781066C>T , CM000672.2:g.110781066C>T GRCh38
NC_000010.10:g.112540824C>T , CM000672.1:g.112540824C>T GRCh37
NC_000010.9:g.112530814C>T NCBI36
NG_021177.1:g.141670C>T , LRG_382:g.141670C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369519.4:c.457C>T MANE Select ENSP00000358532.3:p.Pro153Ser
ENST00000369519.3:c.457C>T ENSP00000358532.3:p.Pro153Ser
NM_001134363.2:c.457C>T NP_001127835.2:p.Pro153Ser
XM_011539697.1:c.73C>T XP_011537999.1:p.Pro25Ser
XM_017016103.2:c.292C>T XP_016871592.1:p.Pro98Ser
XM_017016104.2:c.73C>T XP_016871593.1:p.Pro25Ser
NM_001134363.3:c.457C>T MANE Select NP_001127835.2:p.Pro153Ser